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Butanoic acid, 4-chloro-4-oxo-, ethyl ester → Ethyl 4-(2-thiazolyl)-4-oxobutyrate

HRID 1988762
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반응식

HRID 1988762 반응식
C[Si](C)(C)[C:3]1[S:4][CH:5]=[CH:6][N:7]=1.[CH2:10]([O:12][C:13](=[O:19])[CH2:14][CH2:15][C:16](Cl)=[O:17])[CH3:11].C([O-])(O)=O.[Na+]>C(Cl)Cl>[CH2:10]([O:12][C:13](=[O:19])[CH2:14][CH2:15][C:16](=[O:17])[C:3]1[S:4][CH:5]=[CH:6][N:7]=1)[CH3:11]
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참가 물질

5

반응물 3

HCID 84648Butanoic acid, 4-chloro-4-oxo-, ethyl esterHCID 516892Sodium BicarbonateHCID 5884532-Trimethylsilylthiazole

생성물 1

HCID 68499389Ethyl 4-(2-thiazolyl)-4-oxobutyrate

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a stirred solution of 2-trimethylsilanyl-thiazole (2.6 g, 16.53 mmol) in DCM (30 mL) is added a solution of 3-chlorocarbonyl-propionic acid ethyl ester (5.4 g, 32.81 mmol) in DCM (10 mL). The mixture is stirred overnight at room temperature. To the mixture is added 5% NaHCO3 (30 mL) and mixture is stirred at room temperature for 20 minutes. The organic layer is separated and the aqueous lay is extracted with DCM (2×50 mL). The combined organic layers are dried and the solvent removed. The residue is separated by column (methylene chloride) to give 4-oxo-4-thiazol-2-yl-butyric acid ethyl ester.

후처리

  1. stirringis stirred at room temperature for 20 minutes
  2. customThe organic layer is separated
  3. extractionthe aqueous lay is extracted with DCM (2×50 mL)
  4. customThe combined organic layers are dried
  5. customthe solvent removed
  6. customThe residue is separated by column (methylene chloride)

출처 및 근거

ORD 기록
ord-37e34f4a12de4635b0f7fa48efd0416a
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07642267B2

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