反应 #4142111
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-40c63743c6454f5080e22b1e91a8e8ec暂无可渲染的结构数据
C1=CC(=CC=C1CC(=O)Cl)Br产品信息
4-溴苯乙酰氯(CAS 37859-24-8)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:
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来源 ID: ord-a39e45e9e49142779881ad5c181903b2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of NaH (7.6 g, 158 mmol) in toluene (142 mL) at 0° C. was added dropwise a solution of ethyl isobutylylacetate (20 g, 126 mmol) in toluene (52 mL) and the resulting solution was stirred under an argon atmosphere for 30 min. Then, a solution of 4-bromophenylacetyl chloride (29.4 g, 126 mmol, prepared as described in reference example 1) in toluene (98 mL) was slowly added and the reaction mixture stirred at room temperature overnight. The resulting solution was poured into H2O-EtOAc and extracted with H2O (2×). The organic phase was washed with brine, the aqueous phase was acidified and extracted with EtOAc, and the combined organic phases were dried and concentrated. The residue was chromatographed on silica gel (hexane-EtOAc, 5%) to afford the title compound (29 g, 65%). the reaction mixture stirred at room temperature overnight extracted with H2O (2×) The organic phase was washed with brine extracted with EtOAc the combined organic phases were dried concentrated The residue was chromatographed on silica gel (hexane-EtOAc, 5%)
来源 ID: ord-3194903743c5487f85bcd3797cc1ec6cPubChem References
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