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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1195884생성일: 2026년 10월 27일

Indole → 5-Methoxy-2-methyl-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/1195884

반응식

참여 물질

역할이름HCID투입량
반응물IndoleHCID 798—
반응물DimethylformamideHCID 6228—
반응물Phosphorus oxychlorideHCID 24813—
반응물5-Methoxy-2-methylindoleHCID 70642—
생성물5-Methoxy-2-methyl-1H-indole-3-carbaldehydeHCID 315958098%

반응 조건

온도35 °C

반응 단계

Phosphorous oxychloride (12.7 ml, 0.136 mol) is added dropwise at 0° C. to dimethylformamide (42.4 ml, 0.544 mol) over 30 minutes. A solution of 5-methoxy-2-methylindole (20 g, 0.124 mol) in 40 ml of DMF added dropwise over 45 minutes. When 30 ml of the indole solution has been added, it becomes necessary to add 10 ml of DMF to break up the heavy paste which forms. The reaction mixture is then warmed to 35° C. for one hour. After 30 minutes the reaction again becomes too pasty, and 5 ml more of DMF is added. The bath is removed, and 60 g of crushed ice is added quickly to the reaction mixture. The reaction mixture is stirred for 30 minutes followed by addition of 20 ml of water and 40 g of ice. A solution of sodium hydroxide (25 g) in water (200 ml) is added dropwise to the red solution. After the first one-third of this sodium hydroxide solution has been added, the color changes to yellow, and the remainder of the sodium hydroxide solution is added quickly. It is rapidly brought to a boil (100°-120° C.) for 10 minutes, cooled and refrigerated overnight. The solid is filtered and washed four times with cool water. It is dried in a vacuum oven at 50° C. for 22 hours to give 23.0 g (98%) of powdery yellow crystals of pure 5-methoxy-2-methyl-1H-indole-3-carboxaldehyde; mp 190°-191° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05112846
출처 데이터셋uspto-grants-1992_05
ORD IDord-bad444d74bee40c489f29b522771ca06
출처 메모uspto-grants-1992_05