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p-Anisoyl chloride → 3-(4-Methoxybenzoyl)-4-oxothiazolidine

HRID 34909
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HRID 34909 반응식
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=[O:8])=[CH:5][CH:4]=1.[O:12]=[C:13]1[CH2:17][S:16][CH2:15][NH:14]1.C(N(CC)CC)C>O1CCCC1>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([N:14]2[C:13](=[O:12])[CH2:17][S:16][CH2:15]2)=[O:8])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7477p-Anisoyl chlorideHCID 8471TriethylamineHCID 6375914-Thiazolidinone

생성물 1

HCID 138539863-(4-Methoxybenzoyl)-4-oxothiazolidine수율 62.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 4-methoxybenzoyl chloride (20.7 g) in tetrahydrofuran (50 ml) was added dropwise to a mixture of 4-oxo-thiazolidine (12.5 g) and triethylamine (16.9 ml) in tetrahydrofuran (200 ml) at -5° C. with stirring. The mixture was stirred at that temperature for 3 hours and at room temperature for 4 hours, and allowed to stand overnight. After the solvent was evaporated in vacuo, the residue was mixed with water and extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate and then with water, dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from a mixture of ethyl acetate and n-hexane to give 3-(4-methoxybenzoyl)-4-oxothiazolidine (18.1 g) as slightly brown prisms.

후처리

  1. stirringThe mixture was stirred at that temperature for 3 hours and at room temperature for 4 hours
  2. customAfter the solvent was evaporated in vacuo
  3. additionthe residue was mixed with water
  4. extractionextracted with ethyl acetate
  5. washThe extract was washed with saturated aqueous sodium hydrogen carbonate
  6. dry with materialwith water, dried over magnesium sulfate
  7. customevaporated in vacuo
  8. customThe residue was recrystallized from a mixture of ethyl acetate and n-hexane

출처 및 근거

ORD 기록
ord-2ff8a32f1b9e40a49bf580642295e58a
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04764514

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