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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 1030110
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HRID 1030110 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
  4. additionBenzene (10 ml) was added
  5. customthe mixture was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-9526b21a2f9149768b8fd585de14c167
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05104886

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