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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413885생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 1-(3-Dimethylaminophenyl)-2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/413885

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물TriethylamineHCID 8471—
반응물1,3-Benzenediamine, N1,N1-dimethyl-, hydrochloride (1:2)HCID 77124—
반응물Ethyl 2-acetyl-4-oxo-4-phenylbutanoateHCID 312893—
용매EthanolHCID 702—
생성물1-(3-Dimethylaminophenyl)-2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 10132496—

반응 단계

N,N-dimethyl-1,3-phenylenediamine dihydrochloride (5 mmol, 1.0 g), triethylamine (10 mmol, 1.4 mL), 3-oxo-2-(2-oxo-2-phenyl-ethyl)-butyric acid ethyl ester (5 mmol, 1.2 g), and tosic acid (0.1 g) were combined in ethanol (25 mL), then heated under reflux (12 hrs). The solvents were removed under vacuum, the resulting oil was redissolved in methylene chloride, then applied to a silica column. The purified product was collected as a translucent oil. The named compound was identified by 1H-NMR (CDCl3, ppm): 1.28 t (3H), 2.35 s (3H), 2.77 s (6H), 4.2 q (2H), 6.3-6.7 m (4H), and 7.0-7.3 m (5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06569890B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-1018c1edffcf433f8cded781d00d00c1
출처 메모uspto-grants-2003_05