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

HRID 34911
ノート
印刷プレビュー

反応式

HRID 34911 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 74014-Methoxybenzenesulfonyl chlorideHCID 24758Sodium hydrideHCID 6375914-Thiazolidinone

生成物 1

HCID 138540063-(4-Methoxybenzenesulfonyl)-4-oxothiazolidine収率 41.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8b82961fc33c472597258e60e2e37873
出典データセット
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04764514

反応ノート

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