反应 #4080574
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-0e4884d5ff734762b41432c6aaef0c4a暂无可渲染的结构数据
CCCCCCCCOC1=CC=C(C=C1)CO产品信息
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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-0e4884d5ff734762b41432c6aaef0c4a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8829f34e486d41a096a73f3cbf100a0c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ffa42fafbcb04fe293a23ab509539079反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3b14015a334c4da99a34dfd72b2bf869反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Diethyl azodicarboxylate (18.4 g) was added dropwise to a suspension of 4-octyloxybenzyl alcohol (25 g), N-hydroxyphthalimide (17.15 g) and triphenylphosphine (27.74 g) in tetrahydrofuran (250 ml) under ice-cooling. The reaction mixture was stirred at room temperature for 2 hours, and evaporated in vacuo. The residue was purified by chromatography on silica gel to give N-(4-octyloxybenzyloxy)phthalimide (33.45 g) as crystals. cooling evaporated in vacuo The residue was purified by chromatography on silica gel
来源 ID: ord-e527255a53ed4f3889660a581d775414反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Diethyl azodicarboxylate (18.4 g) was added dropwise to a suspension of 4-octyloxybenzyl alcohol (25 g), N-hydroxyphthalimide (17.15 g) and triphenylphosphine (27.74 g) in tetrahydrofuran (250 ml) under ice-cooling. The reaction mixture was stirred at room temperature for 2 hours, and evaporated in vacuo. The residue was purified by chromatography on silica gel to give N-(4-octyloxybenzyloxy)phthalimide (33.45 g) as crystals. cooling evaporated in vacuo The residue was purified by chromatography on silica gel
来源 ID: ord-e527255a53ed4f3889660a581d775414反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of lithium aluminum hydride (4.05 g) in tetrahydrofuran (475 ml) was added dropwise a solution of 4-octyloxybenzaldehyde (25 g) in tetrahydrofuran (25 ml) at 55°-60° C. The reaction mixture was stirred under reflux for 1 hour. Thereto, sodium fluoride (35.84 g) and water (11.52 ml) were added under ice-cooling. The mixture was stirred for 30 minutes, and filtered. The filtrate was evaporated in vacuo to give 4-octyloxybenzyl alcohol (25.1 g) as crystals. under reflux for 1 hour cooling The mixture was stirred for 30 minutes filtered The filtrate was evaporated in vacuo
来源 ID: ord-3d18488ea63c4315ac4bebc64d9f60fd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0e4884d5ff734762b41432c6aaef0c4a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8829f34e486d41a096a73f3cbf100a0c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ffa42fafbcb04fe293a23ab509539079反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3b14015a334c4da99a34dfd72b2bf869反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This compound was synthesized following the same general procedure as that for the preparation of 4-ethoxybenzyl chloride; thionyl chloride (6.36 g, 53.4 mmol), 4-octyloxybenzyl alcohol (12.4 g, 52.5 mmol), CH2Cl2 (150 mL). This compound was synthesized
来源 ID: ord-2efc181edf924ec9a8b065fcbc3c2897PubChem References
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