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2-[p-(Benzyloxy)phenoxy]propionaldehyde → 2-(4-Hydroxyphenoxy)propanal

HRID 249203
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HRID 249203 반응식
C([O:8][C:9]1[CH:19]=[CH:18][C:12]([O:13][CH:14]([CH3:17])[CH:15]=[O:16])=[CH:11][CH:10]=1)C1C=CC=CC=1>C(O)C.[Pd]>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([O:13][CH:14]([CH3:17])[CH:15]=[O:16])=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 189627142-[p-(Benzyloxy)phenoxy]propionaldehyde

생성물 1

HCID 189627082-(4-Hydroxyphenoxy)propanal수율 36.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of 2-[p-(benzyloxy)phenoxy]propionaldehyde (34.6 g, 0.135 mol) and 5% Pd on carbon (2.0 g) in ethanol (250 mL) is placed on a Parr hydrogenerator. Over 5 hours, the pressure drops from 37 psi to 28 psi. The reaction mixture is then filtered through celite and concentrated in vacuo to obtain a dark yellow syrup. Flash chromatography of the syrup using silica gel and eluting with methylene chloride followed by 1% to 10% ethyl acetate in methylene chloride gives the title product as a dark yellow syrup (8.2 g) which is identified by 1H NMR spectral analysis.

후처리

  1. filtrationThe reaction mixture is then filtered through celite and
  2. concentrationconcentrated in vacuo
  3. customto obtain a dark yellow syrup
  4. washeluting with methylene chloride

출처 및 근거

ORD 기록
ord-304c5e9c0b1c4e70b7f6b8167b4c6617
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05213606

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