反应 #4149946
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-dc892b3fbf1a45e495d4db744ce9d964暂无可渲染的结构数据
C1=CC(=C(C(=C1)Br)Cl)F产品信息
1-溴-2-氯-3-氟苯(CAS 883499-24-9)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-dc892b3fbf1a45e495d4db744ce9d964反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4719af450ec74e24984d0d5d4aa92dc0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-955061959e2d43dc9aed1400073dd6b2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-dfe8bb1213334c1691cac45060d76e64反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d928fbdeeffc4fb99c20a4b47403482e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To stirred phenyl-methanethiol (14.8 g, 119.36 mmol) in 175 ml DMF was added Cs2CO3 (38.89 g, 119.36 mmol) under argon. After 10 min 1-bromo-2-chloro-3-fluoro-benzene (25 g, 119.36 mmol) in 25 ml DMF was added and stirring was continued overnight at RT and then 3 h at 80° C. After cooling the mixture was diluted with ethyl acetate/water and washed subsequently with 1 N HCl and brine. The organic layer was dried with MgSO4, filtered and evaporated. Purification by chromatography on silica gel yielded 22 g (59%) as an amorphous, colorless solid. 3 h at 80° C After cooling the mixture washed subsequently with 1 N HCl and brine The organic layer was dried with MgSO4 filtered evaporated Purification by chromatography on silica gel yielded 22 g (59%) as an amorphous, colorless solid
来源 ID: ord-74b1cc83ce50408187a4c429807761ed反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-dc892b3fbf1a45e495d4db744ce9d964反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4719af450ec74e24984d0d5d4aa92dc0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4719af450ec74e24984d0d5d4aa92dc0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To stirred phenyl-methanethiol (14.8 g, 119.36 mmol) in 175 ml DMF was added Cs2CO3 (38.89 g, 119.36 mmol) under argon. After 10 min 1-bromo-2-chloro-3-fluoro-benzene (25 g, 119.36 mmol) in 25 ml DMF was added and stirring was continued overnight at RT and then 3 h at 80° C. After cooling the mixture was diluted with ethyl acetate/water and washed subsequently with 1 N HCl and brine. The organic layer was dried with MgSO4, filtered and evaporated. Purification by chromatography on silica gel yielded 22 g (59%) as an amorphous, colorless solid. 3 h at 80° C After cooling the mixture washed subsequently with 1 N HCl and brine The organic layer was dried with MgSO4 filtered evaporated Purification by chromatography on silica gel yielded 22 g (59%) as an amorphous, colorless solid
来源 ID: ord-74b1cc83ce50408187a4c429807761ed反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-955061959e2d43dc9aed1400073dd6b2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d928fbdeeffc4fb99c20a4b47403482ePubChem 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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