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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1461438생성일: 2026년 10월 27일

4-Chlorobenzoyl chloride → 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-carboxaldehyde

https://huagongshe.com/reaction/1461438

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorobenzoyl chlorideHCID 8501—
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물5-Methoxy-2-methyl-1H-indole-3-carbaldehydeHCID 3159580—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-carboxaldehydeHCID 1089278782.6%

반응 조건

온도-60 °C

반응 단계

To a solution of 5-methoxy-2-methyl-lH-indole-3-carboxaldehyde (20 g, 106 mmol) in 210 ml of dry dimethylformamide is added oil free sodium hydride (2.7 g, 111 mmol). The reaction mixture is stirred for five hours at which time it is cooled to -60° C., and freshly distilled 4-chlorobenzoyl chloride (14.4 ml, 117 mmol) is added dropwise. It is stirred for an additional 10 minutes and worked up by pouring the cold paste into cold ethyl acetate and water. The organic phase is washed once with dilute sodium bicarbonate solution, once again with water, and once with a saturated solution of sodium chloride. It is further dried with magnesium sulfate, filtered, and concentrated in vacuo to a solid which is stirred vigorously with 50 ml of methanol for two hours. The solid is filtered and dried to give 1-(4-chlorobenzoyl) -5-methoxy-2-methyl-lH-indole-3-carboxaldehyde (28.7 g, 82.5%). A portion which is recrystallized from ethyl acetate has a mp of 150.5°- 151.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05075330
출처 데이터셋uspto-grants-1991_12
ORD IDord-99a361a9d8a34e6796b346f295ddb41b
출처 메모uspto-grants-1991_12