反应 #4164928
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-08a7635a464c40cfb6fec0b4423ee7b5暂无可渲染的结构数据
C(C(=O)Cl)(Br)Br产品信息
Dibromoacetyl chloride(CAS 5302-76-1)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-08a7635a464c40cfb6fec0b4423ee7b5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-aad1c64cf4b04f6090512acd701442fe反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-08a7635a464c40cfb6fec0b4423ee7b5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in an ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil. To a mixture of 3.5 g was added 3.1 g continued cooling When reaction the benzene layer separated dried over magnesium sulfate the benzene removed under vacuum
来源 ID: ord-488588d65d84447d94e5a6264ceca35c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in an ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil. To a mixture of 3.5 g was added 3.1 g continued cooling When reaction the benzene layer separated dried over magnesium sulfate the benzene removed under vacuum
来源 ID: ord-488588d65d84447d94e5a6264ceca35c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in an ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil. To a mixture of 3.5 g was added 3.1 g continued cooling When reaction the benzene layer separated dried over magnesium sulfate the benzene removed under vacuum
来源 ID: ord-b7da4a5170a44d28aa926a194af50f8f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in an ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil. To a mixture of 3.5 g was added 3.1 g continued cooling When reaction the benzene layer separated dried over magnesium sulfate the benzene removed under vacuum
来源 ID: ord-b7da4a5170a44d28aa926a194af50f8f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-aad1c64cf4b04f6090512acd701442fe反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil. To a mixture of 3.5 g was added 3.1 g continued cooling When reaction the benzene layer separated dried over magnesium sulfate the benzene removed under vacuum
来源 ID: ord-018ee021580b425b9dcb6d7a037296b8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil. To a mixture of 3.5 g was added 3.1 g continued cooling When reaction the benzene layer separated dried over magnesium sulfate the benzene removed under vacuum
来源 ID: ord-018ee021580b425b9dcb6d7a037296b8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil. To a mixture of 3.5 g was added 3.1 g continued cooling When reaction the benzene layer separated dried over magnesium sulfate the benzene removed under vacuum
来源 ID: ord-018ee021580b425b9dcb6d7a037296b8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 3.5 g. of 2,2-dimethyl thiazolidine, 50 ml. of benzene and 7.1 g. of dibromoacetyl chloride mixed in an ice bath was added 3.1 g. of triethylamine dropwise with stirring and continued cooling. When reaction was complete, the mixture was poured into watwer and the benzene layer separated, dried over magnesium sulfate and the benzene removed under vacuum. Yield was 8.5 g. of a dark oil. To a mixture of 3.5 g was added 3.1 g continued cooling When reaction the mixture was poured into watwer the benzene layer separated dried over magnesium sulfate the benzene removed under vacuum
来源 ID: ord-9fdcb91d3ecf463ca31c2f273ca8846cPubChem References
以下资料来自该化合物的公开数据库参考记录。
