돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 913965생성일: 2026년 10월 27일

1-Nitropropane → 7-bromo-5-chloro-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/913965

반응식

참여 물질

역할이름HCID투입량
반응물1-NitropropaneHCID 7903—
반응물Ammonium phosphate, tribasicHCID 159282—
반응물7-bromo-5-chloro-1H-indole-3-carbaldehydeHCID 57546113—
용매Acetic AcidHCID 176—
생성물7-bromo-5-chloro-1H-indole-3-carbonitrileHCID 5754622054.5%

반응 단계

A mixture of 7-bromo-5-chloro-1H-indole-3-carbaldehyde (0.80 g, 3.09 mmol), Ammonium phosphate, dibasic (1.269 mL, 15.47 mmol), and 1-nitropropane (0.276 mL, 3.09 mmol) in Acetic Acid (20 mL) was heated at reflux. The solvent was evaporated, the residue was taken up in aqueous sodium bicarbonate (300 mL) and extracted with ethyl acetate (3×20 mL). The organic layers were dried with MgSO4 and evaporated. The residue was purified by chromatography on SiO2 with 20%-25% ethyl acetate/hexanes to give 7-bromo-5-chloro-1H-indole-3-carbonitrile (0.43 g, 1.683 mmol, 54.4% yield) as a yellow solid. 1H-NMR (CDCl3, 400 MHz) δ 8.27 (bs, 1H), 7.79 (s, 1H), 7.72 (d, J=1.8 Hz, 1H), 7.49 (d, J=1.8 Hz, 1H). LC/MS (HPLC method 4): tR=3.12 min, 255.01(MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08026257B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-b014e68c04824017b8e7a4fd2023d96d
출처 메모uspto-grants-2011_09