反应 #4012757
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8ce9b0160f2f40ef89e12ebf41ba1eda暂无可渲染的结构数据
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8ce9b0160f2f40ef89e12ebf41ba1eda反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of monodispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of monodispersed tetraethylene glycol monobenzylether 24 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed; CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the monodispersed compound 25 as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed; CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-6bc6989e0099498ea1828ed88504fb39反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of monodispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of monodispersed tetraethylene glycol monobenzylether 24 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the monodispersed compound 25 as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-19fa7e8ca039452aba5342ebd9d2c51f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of monodispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of monodispersed tetraethylene glycol monobenzylether 24 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the monodispersed compound 25 as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-bded469b88e2406ea6270ef181b71f85反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of monodispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of monodispersed tetraethylene glycol monobenzylether 24 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the monodispersed compound 25 as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-278eccf31d4f4cae9aba084883275375反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of monodispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of monodispersed tetraethylene glycol monobenzylether 24 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the monodispersed compound 25 as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-278eccf31d4f4cae9aba084883275375反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of non-polydispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of non-polydispersed tetraethylene glycol monobenzylether 40 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the non-polydispersed title compound as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-1645c19f06e3453d9f309ee681ad518c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of non-polydispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of non-polydispersed tetraethylene glycol monobenzylether 40 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the non-polydispersed title compound as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-26e75621b35249a29877c32d5ebb71b6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of non-polydispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of non-polydispersed tetraethylene glycol monobenzylether 40 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the non-polydispersed title compound as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-746ede52140b4ff6b3a407b25a39a3df反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of non-polydispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of non-polydispersed tetraethylene glycol monobenzylether 40 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the non-polydispersed title compound as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-b2cbf350d667459bb6ec706b7b02f558反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8ce9b0160f2f40ef89e12ebf41ba1eda反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of non-polydispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of non-polydispersed tetraethylene glycol monobenzylether 40 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the non-polydispersed title compound as a clear oil (2.62 g, 34% yield). was added dropwise the reaction mixture was stirred overnight The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) the filtrate was washed H2O, dried MgSO4 evaporated to dryness The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) chromatographed (silica, chloroform/methanol, 25:1)
来源 ID: ord-1645c19f06e3453d9f309ee681ad518cPubChem References
以下资料来自该化合物的公开数据库参考记录。
