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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1512755생성일: 2026년 10월 26일

Dimethylformamide → 4-fluoro-3-formyl-1H-indole-7-carbonitrile

https://huagongshe.com/reaction/1512755

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ethyl AcetateHCID 8857—
반응물Oxalyl chlorideHCID 65578—
반응물4-Fluoro-1H-indole-7-carbonitrileHCID 22473022—
용매DichloromethaneHCID 6344—
생성물4-fluoro-3-formyl-1H-indole-7-carbonitrileHCID 5914617985.1%

반응 단계

To a solution of (COCl)2 (16.0 g) in DCM (200 mL) at 0° C. was added a solution of DMF (6 mL) in DCM (50 mL) dropwise. Half an hour later, a solution of 4-fluoro-1H-indole-7-carbonitrile (D41) (11.0 g) in DCM (60 mL) was added. The reaction was allowed to warm to RT to form a yellow precipitate. After 6 h the solvent was removed by evaporation. Then THF (100 mL) and 2M aqueous NaOH (100 L) were added to the residue obtained above. After being stirred for about 1 hour, EtOAc (1 L) was added. The organic phase was separated and the aqueous phase was extracted with EtOAc. The combined organic solution was dried over anhydrous sodium sulfate. The dried solution was concentrated to afford 4-fluoro-3-formyl-1H-indole-7-carbonitrile (D42) as a yellow solid (11.0 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08217028B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-df697b7135ed4f2ea17eb24c2e6d36aa
출처 메모uspto-grants-2012_07