Dichloromethane → 3-(3-Phenylsulfamoylphenyl)acryloyl chloride

HRID 351031ノート

反応式

HRID 351031 の反応式
[C:1]1([NH:7][S:8]([C:11]2[CH:12]=[C:13]([CH:17]=[CH:18][C:19]([OH:21])=O)[CH:14]=[CH:15][CH:16]=2)(=[O:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:22]CCl>CN(C)C=O>[C:1]1([NH:7][S:8]([C:11]2[CH:12]=[C:13]([CH:17]=[CH:18][C:19]([Cl:22])=[O:21])[CH:14]=[CH:15][CH:16]=2)(=[O:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

参加物

4

反応物 2

HCID 6344DichloromethaneHCID 670195203-(3-Phenylsulfamoylphenyl)acrylic acid

生成物 1

HCID 739894323-(3-Phenylsulfamoylphenyl)acryloyl chloride収率 100.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide触媒

反応条件

温度
40 °C

実験手順

To a suspension of 3-(3-phenylsulfamoylphenyl)acrylic acid (5a) (0.173 g, 0.57 mmol) in dichloromethane (2.3 ml) oxalyl chloride (0.17 ml, 1.95 mmol) and one drop of dimethylformamide were added. The reaction mixture was stirred at 40° C. for one hour and concentrated under reduced pressure to give crude title compound (0.185 g).

後処理

  1. additionwere added
  2. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-8ac4c2cf393d479a98c3734096bb6b8c
出典データセット
uspto-grants-2007_02
特許番号
US07183298B2

反応ノート

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