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2-(2',3'-Dimethoxyphenyl)-1-furanylethanone → 2-(2',3'-Dimethoxyphenyl)-1-tetrahydrofuranyl ethanol

HRID 54139
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인쇄 미리보기

반응식

HRID 54139 반응식
[CH3:1][O:2][C:3]1[C:8]([O:9][CH3:10])=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:11][C:12]([C:14]1[O:15][CH:16]=[CH:17][CH:18]=1)=[O:13].[H][H]>[Pd].CO>[CH3:1][O:2][C:3]1[C:8]([O:9][CH3:10])=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:11][CH:12]([CH:14]1[CH2:18][CH2:17][CH2:16][O:15]1)[OH:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 199612172-(2',3'-Dimethoxyphenyl)-1-furanylethanoneHCID 178418361HCID 178418361, 화합물2회

생성물 1

HCID 199611152-(2',3'-Dimethoxyphenyl)-1-tetrahydrofuranyl ethanol수율 70.5%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A solution of 450 mg(1.8 mmol) of 2-(2',3'-dimethoxyphenyl)-1-furanylethanone, from Step 2, and 20% palladium on carbon (225 mg) in 75 mL of methanol was shaken under 4 atmospheres of hydrogen until hydrogen uptake ceased. The solution was filtered and concentrated in vacuo to give 320 mg (69% yield) of the title compound as an oily solid. This product was carried on without purification to the next step.

후처리

  1. filtrationThe solution was filtered
  2. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-8c04c4ddd0734cad882f9e5058c66578
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05621133

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