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2,5-Dihydro-2,5-dimethoxy-3-phenylfuran → 2,5-Dimethoxy-3-phenyltetrahydrofuran

HRID 382133
노트
인쇄 미리보기

반응식

HRID 382133 반응식
[CH3:1][O:2][CH:3]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:6][CH:5]([O:14][CH3:15])[O:4]1>CCOC(C)=O.[Rh]>[CH3:1][O:2][CH:3]1[CH:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:6][CH:5]([O:14][CH3:15])[O:4]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 183803672,5-Dihydro-2,5-dimethoxy-3-phenylfuran

생성물 1

HCID 185488262,5-Dimethoxy-3-phenyltetrahydrofuran수율 98%

시약·촉매·용매 2

HCID 23948Rhodium촉매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 2,5-dihydro-2,5-dimethoxy-3-phenylfuran (590 mg, 2.86 mmol) and 10% Rh/Al2O3 (110 mg) in EtOAc (10 mL) was stirred under H2 atmosphere for 24 hours. The catalyst was filtered onto Celite and rinsed with EtOAc. The filtrate was concentrated in vacuo to afford 583 mg (98%) of 2,5-dimethoxy-3-phenyl-tetrahydrofuran as a colorless oil which was typically used without further purification.

후처리

  1. filtrationThe catalyst was filtered onto Celite
  2. washrinsed with EtOAc
  3. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-8792c64d56494174b278534e84dcc627
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06306892B1

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