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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2396561생성일: 2026년 10월 25일

ANILINE, p-CHLORO-N-METHYL-N-NITROSO- → 5-Chloro-1-methyl-3-phenylindole-2-acetic acid

https://huagongshe.com/reaction/2396561

반응식

참여 물질

역할이름HCID투입량
반응물ANILINE, p-CHLORO-N-METHYL-N-NITROSO-HCID 13874—
반응물Ethyl 3-oxo-4-phenylbutanoateHCID 225855—
반응물Sodium AcetateHCID 517045—
반응물1-(4-Chlorophenyl)-1-methyl hydrazine hydrochlorideHCID 18987490—
촉매ZincHCID 23994—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물5-Chloro-1-methyl-3-phenylindole-2-acetic acidHCID 15410730—

반응 단계

To a solution of γ-phenyl acetoacetic acid ethyl ester (2.88 g) in a mixture of acetic acid (30 ml) and water (10 ml) were added sodium acetate (1.83 g) and 1-(4-chlorophenyl)-1-methyl hydrazine hydrochloride (2.73 g) {prepared from 4-chloro-N-methyl-N-nitroso aniline by subjecting to reduction with zinc powder in a mixture of acetic acid and water [m.p.171°-174° C.; NMR (200 MHz, DMSO-d6) ppm: 3.14(3H,s), 7.20(2H,d,J=9 Hz), 7.29(2H,d,J=9 Hz)]}. The mixture was stirred for 15 minutes at room temperature, then for 20 minutes at 110° C. The reaction mixture was concentrated, which was dissolved in ethyl acetate. The solution was washed with water, dilute hydrochloric acid, water, an aqueous solution of sodium hydrogencarbonate and water, successively, which was then dried, followed by distilling off the solvent. The residue was purified by means of a silica gel (30 g) column chromatography (hexane-ethyl acetate=4:1) to give ethyl ester of 5-chloro-1-methyl-3-phenylindole-2-acetic acid as an oily substance (4.34 g). [NMR (200 MHz, CDCl3) ppm: 10 1.29(3H,t,J=7 Hz), 3.76(3H,s), 3.86(2H,s), 4.24(2H,q,J=7 Hz), 7.17-7.62(8H,m)]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05492929
출처 데이터셋uspto-grants-1996_02
ORD IDord-a951888c422d49768afa6ca3cd75704c
출처 메모uspto-grants-1996_02