Ethyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate → (2-Chloro-4-(trifluoromethyl)thiazol-5-yl)methanol

HRID 354724노트

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HRID 354724 반응식
[Cl:1][C:2]1[S:3][C:4]([C:11](OCC)=[O:12])=[C:5]([C:7]([F:10])([F:9])[F:8])[N:6]=1.C([BH3-])#N.[Na+].[BH4-].[Na+]>C(O)C>[Cl:1][C:2]1[S:3][C:4]([CH2:11][OH:12])=[C:5]([C:7]([F:8])([F:9])[F:10])[N:6]=1

참가 물질

5

실험 절차

To a mixture of 2.6 g (0.01 mol) of ethyl 2-chloro-4-(trifluoromethyl)-5-thiazolecarboxylate and 10 ml of ethanol was added 0.62 g of sodium cyanoborohydride. The reaction mixture was stirred for 5 minutes and 0.40 g of sodium borohydride was added. The temperature of the reaction mixture raised spontaneously to boiling point. The reaction mixture was stirred for 30 minutes and quenched with water. The aqueous mixture was extracted with ether. The ether solution was dried over CaSO4 and concentrated under reduced pressure. The residue was crystallized from petroleum ether to give 1.6 g (74%) of 2-chloro-4-(trifluoromethyl)-5-thiazolemethanol, mp 39°-45° C.

후처리

  1. temperatureThe temperature of the reaction mixture raised spontaneously
  2. stirringThe reaction mixture was stirred for 30 minutes
  3. customquenched with water
  4. extractionThe aqueous mixture was extracted with ether
  5. dry with materialThe ether solution was dried over CaSO4
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was crystallized from petroleum ether

출처 및 근거

ORD 기록
ord-1cfabf648c5d4040808d98934a2d27c5
출처 데이터셋
uspto-grants-1983_03
특허 번호
US04377054

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