6-Hydroxymethylindole → 1H-Indole-6-carboxaldehyde
반응식
[OH:1][CH2:2][C:3]1[CH:11]=[C:10]2[C:6]([CH:7]=[CH:8][NH:9]2)=[CH:5][CH:4]=1>C(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH:2]([C:3]1[CH:11]=[C:10]2[C:6]([CH:7]=[CH:8][NH:9]2)=[CH:5][CH:4]=1)=[O:1]참가 물질
4
실험 절차
Manganese dioxide (240 g) was added to a mechanically stirred solution of 6-hydroxymethylindole (40.7 g) in methylene chloride (1.6 liter). The mixture was stirred for 18 hr, filtered through a pad of diatomaceous earth, the filter cake washed with methylene chloride and chloroform, and the filtrate evaporated to give 6-formylindole (30.55 g) as a yellow solid. The filter cake was washed with tetrahydrofuran and the washings evaporated to give a further crop of 6-formylindole (2.35 g, 82% combined yield); partial NMR (250 MHz, DMSO-d6): 6.58(m, 1H, H3 -indole), 10.00(s, 1H, CHO), 11.71(br s, 1H, NH).
후처리
- filtrationfiltered through a pad of diatomaceous earth
- washthe filter cake washed with methylene chloride and chloroform
- customthe filtrate evaporated
출처 및 근거
- ORD 기록
- ord-27cd4d962190435db17d3ab2c9a33f3b
- 출처 데이터셋
- uspto-grants-1990_01
- 특허 번호
- US04894386
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