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2-Hydroxymethyl-1-methyl-4,5,6-trimethoxyindole → 1-Methyl-4,5,6-trimethoxyindole-2-carboaldehyde

HRID 987448
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반응식

HRID 987448 반응식
[OH:1][CH2:2][C:3]1[N:4]([CH3:18])[C:5]2[C:10]([CH:11]=1)=[C:9]([O:12][CH3:13])[C:8]([O:14][CH3:15])=[C:7]([O:16][CH3:17])[CH:6]=2>C1C=CC=CC=1.[O-2].[O-2].[Mn+4]>[CH3:18][N:4]1[C:5]2[C:10](=[C:9]([O:12][CH3:13])[C:8]([O:14][CH3:15])=[C:7]([O:16][CH3:17])[CH:6]=2)[CH:11]=[C:3]1[CH:2]=[O:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 218916442-Hydroxymethyl-1-methyl-4,5,6-trimethoxyindole

생성물 1

HCID 218916451-Methyl-4,5,6-trimethoxyindole-2-carboaldehyde

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 241Benzene용매

실험 절차

2-Hydroxymethyl-1-methyl-4,5,6-trimethoxyindole (861 mg) was dissolved in benzene (50 mL), activated manganese dioxide (8.7 g) was added to the solution, and the mixture was stirred at room temperature for 2 hours. After the reaction mixture was filtered, and the filtrate was concentrated, the residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:2) to obtain the title compound.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. filtrationAfter the reaction mixture was filtered
  2. concentrationthe filtrate was concentrated
  3. customthe residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:2)

출처 및 근거

ORD 기록
ord-7305eb68cfdf483cbb1fc4b6589a91ca
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06632810B2

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