反应 #4094765
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-81d5be5b44d444a7a59e57fe52a23725暂无可渲染的结构数据
C1=CC=C(C=C1)CCC(CO)(F)F产品信息
2,2-二氟-4-苯基丁-1-醇(CAS 177996-67-7)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-81d5be5b44d444a7a59e57fe52a23725反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-307e09673a714e82a82d085be8aa347f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3cd93de3a86d4345adde4b454e085d38反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Obtained from Intermediate 67 (4.35 g, 19 mmol) by the procedure described in Intermediate 2. The title compound was obtained (3.19 g, 90%) as oil.
来源 ID: ord-ff86116b55354dc48792f2ddb0053355反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Obtained from Intermediate 48 (21.1 g, 75.8 mmol) by the procedure described in Intermediate 2. The title compound was obtained (17.2 g, 96%) as oil.
来源 ID: ord-b5015aeb375948a7829e37f434b381c5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Obtained from Intermediate 40 (1.0 g, 2.85 mmol) by the procedure described in Intermediate 2. Purification by column chromatography with silica gel and n-hexane/ethyl acetate (from 10:1 to 5:1) as eluent gave the title compound (0.68 g, 82%) as oil, Purification by column chromatography with silica gel and n-hexane/ethyl acetate (from 10:1 to 5:1) as eluent
来源 ID: ord-0f1d6bbd9f4544e599e45409a21e37ff反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Obtained from Intermediate 28 (9.5 g, 40 mmol) by the procedure described in Intermediate 2. The title compound was obtained (5.55 g, 80%) as oil.
来源 ID: ord-2fb2a175e8de4ff5abdfd927db8f8cff反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of Intermediate 2 (0.60 g, 3.22 mmol) in 1,6-dibromohexane (1.74 mL, 11.27 mmol) was added tetrabutylammonium bromide (21 mg, 0.064 mmol) and 50% sodium hydroxide (1.2 mL). The mixture was stirred at room temperature overnight. The crude reaction was diluted with n-hexane (20 mL), washed with water (2×10 mL), dried (Na2SO4), and the solvent removed under reduced pressure. The title compound was obtained (2.1 g, 52% purity) and was used in the next step without further purification. The crude reaction washed with water (2×10 mL) dried (Na2SO4) the solvent removed under reduced pressure
来源 ID: ord-cdb17664084b4a9fbb099a70635ba9e3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-81d5be5b44d444a7a59e57fe52a23725反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-307e09673a714e82a82d085be8aa347f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3cd93de3a86d4345adde4b454e085d38反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of Intermediate 2 (0.60 g, 3.22 mmol) in 1,6-dibromohexane (1.74 mL, 11.27 mmol) was added tetrabutylammonium bromide (21 mg, 0.064 mmol) and 50% sodium hydroxide (1.2 mL). The mixture was stirred at room temperature overnight. The crude reaction was diluted with n-hexane (20 mL), washed with water (2×10 mL), dried (Na2SO4), and the solvent removed under reduced pressure. The title compound was obtained (2.1 g, 52% purity) and was used in the next step without further purification. The crude reaction washed with water (2×10 mL) dried (Na2SO4) the solvent removed under reduced pressure
来源 ID: ord-2bdee748bdcc4f51a95b0b20bf6bfca2PubChem References
以下资料来自该化合物的公开数据库参考记录。
