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(3-Benzyloxy-4-iodophenyl)methanol → 3-(Benzyloxy)-4-iodobenzaldehyde

HRID 250843
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반응식

HRID 250843 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH2:16][OH:17])[CH:12]=[CH:13][C:14]=1[I:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>ClCCl.[O-2].[Mn+2]>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:12]=[CH:13][C:14]=1[I:15])[CH:16]=[O:17])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 45140291(3-Benzyloxy-4-iodophenyl)methanol

생성물 1

HCID 534172453-(Benzyloxy)-4-iodobenzaldehyde수율 54%

시약·촉매·용매 2

HCID 160959Manganese oxide촉매HCID 6344Dichloromethane용매

실험 절차

7.8 g (90 mmol, 5 eq) of manganese oxide are added to a solution of 6.5 g (17.98 mmol, 1 eq) of (3-benzyloxy-4-iodophenyl)methanol in 50 mL of dichloromethane. The reaction medium is stirred for 12 hours at room temperature, and the solid is then filtered off and the solvent is evaporated off. The residual oil is chromatographed on silica gel (8/2 heptane/ethyl acetate). The oil obtained is crystallized from pentane. 3.25 g of 3-benzyloxy-4-iodobenzaldehyde are obtained. Yield=54% for the three steps c, d and e.

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후처리

  1. filtrationthe solid is then filtered off
  2. customthe solvent is evaporated off
  3. customThe residual oil is chromatographed on silica gel (8/2 heptane/ethyl acetate)
  4. customThe oil obtained
  5. customis crystallized from pentane

출처 및 근거

ORD 기록
ord-13eb22f67d1b4435aa2fe080be85e975
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863332B2

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