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N,N-二甲基甲酰胺 → 6-Amino-3-bromo-4-fluoro-2-methylbenzonitrile

HRID 17550
笔记
打印预览

反应方程式

HRID 17550 反应方程式
[Br:1]N1C(=O)CCC1=O.CN(C)C=O.[NH2:14][C:15]1[CH:22]=[C:21]([F:23])[CH:20]=[C:19]([CH3:24])[C:16]=1[C:17]#[N:18]>O>[NH2:14][C:15]1[C:16]([C:17]#[N:18])=[C:19]([CH3:24])[C:20]([Br:1])=[C:21]([F:23])[CH:22]=1
参与物实验过程后处理来源与证据反应笔记

参与物

5

反应物 3

HCID 6228N,N-二甲基甲酰胺HCID 67184N-溴代丁二酰亚胺(NBS)HCID 450790392-Amino-4-fluoro-6-methylbenzonitrile

产物 1

HCID 541071796-Amino-3-bromo-4-fluoro-2-methylbenzonitrile收率 95%

试剂、催化剂与溶剂 1

HCID 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]溶剂

实验过程

N-Bromosuccinimide (16.6 g, 93.3 mmol) was gradually added to an N,N-dimethylformamide (250 ml) solution of 2-amino-4-fluoro-6-methylbenzonitrile (I-264) (14.0 g, 93.3 mmol). After stirring for 6 hours, the reaction liquid was poured into water with ice (750 ml), the precipitated solid was collected by filtration. The solid was washed with water, then dried to obtain the entitled compound (20.2 g, 95%) as a gray solid.

后处理

  1. customthe reaction liquid
  2. filtrationthe precipitated solid was collected by filtration
  3. washThe solid was washed with water
  4. customdried

来源与证据

ORD记录
ord-dc698879c22a4075bb6d951fdb6285db
来源数据集
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
专利号
US07737166B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记