Hydrochloric Acid → 2-Tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylic acid

HRID 9088

반응식

HRID 9088 반응식
C([O:3][C:4]([C:6]1[S:10][C:9]([NH:11][O:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[N:8][C:7]=1[CH3:20])=[O:5])C.[OH-].[K+].Cl>O1CCCC1CCO>[C:16]([O:15][C:13]([O:12][NH:11][C:9]1[S:10][C:6]([C:4]([OH:5])=[O:3])=[C:7]([CH3:20])[N:8]=1)=[O:14])([CH3:19])([CH3:17])[CH3:18]

참가 물질

5

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온도
55 °C

실험 절차

A stirred solution of ethyl-2-tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylate (10 g, 34.95 mmol) in tetrahydrofuran-ethanol (250 mL, 2:3) was treated with a 6N KOH solution (250 mL). The mixture was heated to 55° C. overnight. The solution was cooled to 0° C. and acidified with concd. HCl to pH 1. The solvent was evaporated in vacuo. The residue was washed with water, diethyl ether, dried in vacuo over anhydrous phosphorous pentoxide to obtain the title acid (6 g, 89%) as a white solid.

후처리

  1. temperatureThe solution was cooled to 0° C.
  2. customThe solvent was evaporated in vacuo
  3. washThe residue was washed with water, diethyl ether
  4. dry with materialdried in vacuo over anhydrous phosphorous pentoxide
  5. customto obtain the title acid (6 g, 89%) as a white solid

출처 및 근거

ORD 기록
ord-8e2c9bc4dca442bda6037a7be6b1f8b6
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091223B2

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