Allyl bromide → N-[4-(Allylsulfonyl)phenyl]acetamide

HRID 261156

反応式

HRID 261156 の反応式
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([OH:13])=[O:12])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].C(=O)([O-])O.[Na+].[CH2:19](Br)[CH:20]=[CH2:21]>O>[CH2:21]([S:11]([C:8]1[CH:7]=[CH:6][C:5]([NH:4][C:1](=[O:3])[CH3:2])=[CH:10][CH:9]=1)(=[O:13])=[O:12])[CH:20]=[CH2:19]

参加物

5

実験手順

50 parts of p-acetylaminophenylsulfinic acid and 25 parts of sodium hydrogen carbonate are suspended in 300 parts of water. While stirring intensely 36 parts of allyl bromide is dripped in within three hours at 50° to 60° C. Stirring is continued for another four hours at 60° C. 45 parts of p-allylsulfonylacetanilide is obtained with a melting point of 116° to 118° C.

後処理

  1. customis dripped in within three hours at 50° to 60° C

出典と根拠

ORDレコード
ord-3665d53065634e9283f0125b5181815f
出典データセット
uspto-grants-1979_08
特許番号
US04164500

関連ノート

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