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4-Methoxybenzenesulfonyl chloride → 3-(4-Methoxybenzenesulfonyl)-4-oxothiazolidine

HRID 34911
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HRID 34911 반응식
[H-].[Na+].[O:3]=[C:4]1[CH2:8][S:7][CH2:6][NH:5]1.[CH3:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([S:17](Cl)(=[O:19])=[O:18])=[CH:13][CH:12]=1>O1CCCC1>[CH3:9][O:10][C:11]1[CH:12]=[CH:13][C:14]([S:17]([N:5]2[C:4](=[O:3])[CH2:8][S:7][CH2:6]2)(=[O:19])=[O:18])=[CH:15][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 74014-Methoxybenzenesulfonyl chlorideHCID 24758Sodium hydrideHCID 6375914-Thiazolidinone

생성물 1

HCID 138540063-(4-Methoxybenzenesulfonyl)-4-oxothiazolidine수율 41.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Sodium hydride (60% dispersion in mineral oil) (0.58 g) was added portionwise to a solution of 4-oxothiazolidine (1.50 g) and 4-methoxybenzenesulfonyl chloride (3.01 g) in tetrahydrofuran (30 ml) at 0° C. with stirring and the mixture was stirred for 1 hour at the same temperature. After the solvent was evaporated in vacuo, the residue was mixed with ethyl acetate (10 ml) and water (50 ml) and the resultant precipitate was collected by filtration. The cake was washed with water and diisopropyl ether and recrystallized from a mixture of ethanol and ethyl acetate to give 3-(4-methoxybenzenesulfonyl)-4-oxothiazolidine (1.65 g) as slightly brown prisms.

후처리

  1. stirringthe mixture was stirred for 1 hour at the same temperature
  2. customAfter the solvent was evaporated in vacuo
  3. additionthe residue was mixed with ethyl acetate (10 ml) and water (50 ml)
  4. filtrationthe resultant precipitate was collected by filtration
  5. washThe cake was washed with water and diisopropyl ether
  6. customrecrystallized from a mixture of ethanol and ethyl acetate

출처 및 근거

ORD 기록
ord-8b82961fc33c472597258e60e2e37873
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04764514

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