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2-[4-(Hydroxymethyl)phenyl]propan-2-ol → 4-(2-Hydroxypropan-2-yl)benzaldehyde

HRID 2060596
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HRID 2060596 반응식
[OH:1][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([OH:12])([CH3:11])[CH3:10])=[CH:5][CH:4]=1>C(OCC)(=O)C.ClCCl.O=[Mn]=O>[OH:12][C:9]([C:6]1[CH:7]=[CH:8][C:3]([CH:2]=[O:1])=[CH:4][CH:5]=1)([CH3:11])[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 136785732-[4-(Hydroxymethyl)phenyl]propan-2-ol

생성물 1

HCID 104195204-(2-Hydroxypropan-2-yl)benzaldehyde

시약·촉매·용매 3

HCID 14801Manganese dioxide촉매HCID 6344Dichloromethane용매HCID 8857Ethyl Acetate용매

실험 절차

2-[4-(Hydroxymethyl)phenyl]propan-2-ol (1.0 g, 6 mmol) was dissolved in the mixture of ethyl acetate (10 mL) and dichloromethane (5 mL). To the solution, MnO2 (2.6 g, 30 mmol) was added, and the mixture was stirred overnight at room temperature. The solid was filtered off and washed with ethyl acetate. The combined organic phases were concentrated to afford the title compound. 1H NMR (400 MHz CDCl3): δ 10.00 (s, 1H), 7.80 (d, 2H), 7.60 (d, 2H), 1.60 (s, 6H).

후처리

  1. filtrationThe solid was filtered off
  2. washwashed with ethyl acetate
  3. concentrationThe combined organic phases were concentrated

출처 및 근거

ORD 기록
ord-656c0edb794d41698126c70cd4528d6a
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08278335B2

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