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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl 2-(2,2,2-trifluoroethyl)thiazole-4-carboxylate → 2-(2,2,2-Trifluoroethyl)-1,3-thiazole-4-carboxylic acid

HRID 471142
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인쇄 미리보기

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HRID 471142 반응식
[F:1][C:2]([F:15])([F:14])[CH2:3][C:4]1[S:5][CH:6]=[C:7]([C:9]([O:11]CC)=[O:10])[N:8]=1>Cl.O>[F:15][C:2]([F:1])([F:14])[CH2:3][C:4]1[S:5][CH:6]=[C:7]([C:9]([OH:11])=[O:10])[N:8]=1
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참가 물질

4

반응물 1

HCID 57989344Ethyl 2-(2,2,2-trifluoroethyl)thiazole-4-carboxylate

생성물 1

HCID 579889492-(2,2,2-Trifluoroethyl)-1,3-thiazole-4-carboxylic acid

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 962Water용매

반응 조건

온도
80 °C

실험 절차

A mixture of ethyl 2-(2,2,2-trifluoroethyl)thiazole-4-carboxylate (example 67, step c) (0.3 g) in concentrated hydrochloric acid (7 mL) and water (7 mL) was heated at 80° C. for 5 hours under nitrogen. The solvent was evaporated under a stream of nitrogen and the residue partitioned between ethyl acetate (40 mL) and brine (3 mL). The organic layer was dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure to afford the subtitled compound. Yield 0.23 g.

후처리

  1. customThe solvent was evaporated under a stream of nitrogen
  2. customthe residue partitioned between ethyl acetate (40 mL) and brine (3 mL)
  3. dry with materialThe organic layer was dried over sodium sulphate
  4. filtrationfiltered
  5. customthe solvent evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-3ad11f1093ed4264bb13410edb2826a8
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08629271B2

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