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Thionyl Chloride → 2-Chloro-4-methylthiazole-5-carboxylic acid chloride

HRID 1111397
ノート
印刷プレビュー

反応式

HRID 1111397 の反応式
[Cl:1][C:2]1[S:3][C:4]([C:8]([OH:10])=O)=[C:5]([CH3:7])[N:6]=1.S(Cl)([Cl:13])=O>CN(C)C=O>[Cl:1][C:2]1[S:3][C:4]([C:8]([Cl:13])=[O:10])=[C:5]([CH3:7])[N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 6669602-Chloro-4-methyl-1,3-thiazole-5-carboxylic acid

生成物 1

HCID 135933932-Chloro-4-methylthiazole-5-carboxylic acid chloride

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide触媒

実験手順

8.8 g of 2-chloro-4-methylthiazole-5-carboxylic acid was suspended in 7 ml of thionyl chloride, and one drop of N,N-dimethylformamide was added. The mixture was heated under reflux for 1 hour, and then the excess of thionyl chloride was evaporated under reduced pressure Benzene (10 ml) was added, and the mixture was evaporated under reduced pressure. This procedure was repeated three times to give 9.7 g of 2-chloro-4-methylthiazole-5-carboxylic acid chloride which was used in the following reaction without purification.

後処理

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 1 hour
  3. customthe excess of thionyl chloride was evaporated under reduced pressure Benzene (10 ml)
  4. additionwas added
  5. customthe mixture was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-6dd3746899014e568f00fa2e2d74ee0e
出典データセット
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04980363

反応ノート

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