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(8-Methylnaphthalen-1-yl)methanol → 8-Methyl-1-naphthaldehyde

HRID 729782
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HRID 729782 반응식
[CH3:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10]([CH2:12][OH:13])=[CH:9][CH:8]=[CH:7]2>C(Cl)Cl>[CH3:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10]([CH:12]=[O:13])=[CH:9][CH:8]=[CH:7]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 15618201(8-Methylnaphthalen-1-yl)methanol

생성물 1

HCID 155634878-Methyl-1-naphthaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A 1-L 4-neck equipped with an overhead stirrer, a condenser and a thermocouple was charged with 8-methyl-1-napthalenemethanol (18.5 g, 0.107 mol) in CH2Cl2 (500 mL) and stirred at room temperature under N2. Solid Mn(IV)O2 (61 g, 0.7 mol) was carefully added and the reaction was stirred at room temperature for 3 h, then at 40° C. for 6 h and then at room temperature overnight. The reaction mixture was diluted with CH2Cl2 (500 mL), filtered and the filtrate was washed with 1N HCl and then dried over MgSO4. The resulting crude material was purified using silica gel chromatography (8/2 hexane/ethyl acetate) to yield 8-methyl-naphthalene-1-carbaldehyde as a solid.

후처리

  1. stirringthe reaction was stirred at room temperature for 3 h
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customat room temperature
  • customovernight
  • filtrationfiltered
  • washthe filtrate was washed with 1N HCl
  • dry with materialdried over MgSO4
  • customThe resulting crude material was purified
  • 출처 및 근거

    ORD 기록
    ord-09c073ae4fe041d9bf7833299ec62aeb
    출처 데이터셋
    uspto-grants-2009_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07582649B2

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