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2-Benzyloxy-5-[2-(p-toluenesulfonyloxy)ethyl]benzamide → Benzamide

HRID 1862623
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HRID 1862623 반응식
C(O[C:9]1[CH:17]=[CH:16][C:15](CCOS(C2C=CC(C)=CC=2)(=O)=O)=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])C1C=CC=CC=1>CO.O1CCCC1.[C].[Pd]>[C:11]([NH2:13])(=[O:12])[C:10]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 186201132-Benzyloxy-5-[2-(p-toluenesulfonyloxy)ethyl]benzamide

생성물 1

HCID 2331Benzamide수율 260.5%

시약·촉매·용매 3

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

2-Benzyloxy-5-[2-(p-toluenesulfonyloxy)ethyl]benzamide (627 mg) was dissolved in methanol (5 ml) and tetrahydrofuran (5 ml), and 10% palladium carbon (wet, 50% water) (169 mg) was added to the solution. The mixture was stirred for 1 hour at room temperature under a hydrogen atmosphere, and the catalyst was filtered off. Removal of the solvent under reduced pressure gave 2-hydroxy-5-[2-toluenesulfonyloxy)ethyl]benzamide (465 mg).

후처리

  1. filtrationthe catalyst was filtered off
  2. customRemoval of the solvent under reduced pressure

출처 및 근거

ORD 기록
ord-dc26481754074cf99fd4dc34845ef5ad
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06538152B1

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