反应 #4159261
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-c7417a0c5d73423c82890f2ddb1f268b暂无可渲染的结构数据
C1=CC(=C(C=C1Br)CO)Cl产品信息
5-溴-2-氯苯甲醇(CAS 149965-40-2)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c7417a0c5d73423c82890f2ddb1f268b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0a65937a934e42d082be2a5b8e73369b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ba91566e1ee6456290b70acb6f304843反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9288185bf5d34fefb30caa951b104e53反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-611f778a299f4623a3cad07d82797579反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d234168086c64f568bb90a48c0cb22e8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fe86580e532d40519917da0044579795反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Imidazole (5.22 g) and tert-butyldimethylsilyl chloride (8.64 g) were added to a solution of (5-bromo-2-chlorophenyl)methanol (8.47 g) in DMF (80 ml). The reaction mixture was stirred at room temperature overnight. The mixture was diluted with ethyl acetate and washed twice with water. The aqueous layer was again extracted with ethyl acetate. The combined organic layer was washed with brine and dried over anhydrous magnesium sulfate. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography to obtain the title compound (12.6 g). washed twice with water The aqueous layer was again extracted with ethyl acetate The combined organic layer was washed with brine dried over anhydrous magnesium sulfate The filtrate was concentrated under reduced pressure the residue was purified by silica gel column chromatography
来源 ID: ord-5eba45b7fce2423d9641934daf9dc6ad反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of methyl 5-bromo-2-chlorobenzoate (9.23 g) in THF (50 ml) was added dropwise under ice-cooling to a suspension of lithium aluminum hydride (1.42 g) in THF (100 ml). After the completion of addition, the reaction mixture was stirred at room temperature for 45 minutes. Water (1.4 ml), 5N sodium hydroxide solution (1.4 ml) and water (4.2 ml) were sequentially added under ice-cooling to the reaction mixture. The precipitate was removed through Celite and the filtrate was concentrated under reduced pressure to obtain a title compound (7.56 g). After the completion of addition cooling to the reaction mixture The precipitate was removed through Celite the filtrate was concentrated under reduced pressure
来源 ID: ord-a8b97054ece845219ed8c188390ad668反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c7417a0c5d73423c82890f2ddb1f268b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0a65937a934e42d082be2a5b8e73369b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0a65937a934e42d082be2a5b8e73369bPubChem References
以下资料来自该化合物的公开数据库参考记录。
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