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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → 2-Chloro-4-methylthiazole-5-carboxylic acid chloride

HRID 1111397
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HRID 1111397 반응식
[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
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참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 6228Dimethylformamide촉매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-6dd3746899014e568f00fa2e2d74ee0e
출처 데이터셋
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04980363

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