Hydrochloric Acid → 2-Chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acid

HRID 279745노트

반응식

HRID 279745 반응식
[Cl:1][C:2]1[S:3][C:4]([C:11]([O:13]CC)=[O:12])=[C:5]([C:7]([F:10])([F:9])[F:8])[N:6]=1.[OH-].[Na+].O.Cl>O1CCCC1>[Cl:1][C:2]1[S:3][C:4]([C:11]([OH:13])=[O:12])=[C:5]([C:7]([F:9])([F:8])[F:10])[N:6]=1

참가 물질

6

실험 절차

A mixture of 116 g (0.4468 mole) of ethyl 2-chloro-4-trifluoromethyl-5-thiazolecaboxylate, 18 g (0.45 mole) of sodium hydroxide, 200 ml. of water, 400 ml. of tetrahydrofuran was stirred at room temperature for 16 hours and made acidic with 50 ml. of concentrated hydrochloric acid. The reaction mixture was extracted twice with ml. of ether. The ether-tetrahydrofuran solution was dried (MgSO4) and concentrated under reduced pressure. The residual oil was treated with benzene and the benzene solution was concentrated under reduced pressure to remove the last trace of water. The residual solid was recrystallized from hexane-benzene to give 76 g (73.4%) of 2-chloro-trifluoromethyl-5 thiazolecarboxylic acid, m.p. 131°-131.5° C.

후처리

  1. extractionThe reaction mixture was extracted twice with ml
  2. dry with materialThe ether-tetrahydrofuran solution was dried (MgSO4)
  3. concentrationconcentrated under reduced pressure
  4. additionThe residual oil was treated with benzene
  5. concentrationthe benzene solution was concentrated under reduced pressure
  6. customto remove the last trace of water
  7. customThe residual solid was recrystallized from hexane-benzene

출처 및 근거

ORD 기록
ord-50cf5ef5f140483482097a23a4473ba2
출처 데이터셋
uspto-grants-1986_05
특허 번호
US04586948

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