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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47812생성일: 2026년 10월 24일

Hydrochloric Acid → 3-(4-Heptylcarbamoylmethyl-phenyl)-2,2-dimethyl-propionic acid ethyl ester

https://huagongshe.com/ko/reaction/47812

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-HeptanamineHCID 8127—
반응물Thionyl ChlorideHCID 24386—
반응물DiisopropylethylamineHCID 81531—
반응물3-(4-Carboxymethyl-phenyl)-2,2-dimethyl-propionic acid ethyl esterHCID 45116515—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물3-(4-Heptylcarbamoylmethyl-phenyl)-2,2-dimethyl-propionic acid ethyl esterHCID 69884046—

반응 단계

To a stirred solution of 3-(4-carboxymethyl-phenyl)-2,2-dimethyl-propionic acid ethyl ester (0.97 g, 3.67 mmol) in chloroform (15 mL) under an nitrogen atmosphere was added thionyl chloride (11 mmol, 0.804 mL). The mixture was heated under reflux for 2.75 hours, cooled to room temperature and concentrated under reduced pressure to a clear oil. The oil was dissolved in methylene chloride (0.50 mL) then added dropwise to a solution of 1-heptylamine (4.40 mmol, 0.653 mL) and N,N-diisopropylethylamine (4.40 mmol, 0.765 mL) in anhydrous dichloromethane (5 mL) cooled to 0° C. The solution was warmed to room temperature and allowed to stir for 30 minutes, then was poured over a solution of 1 M HCl (10 mL). The aqueous layer was isolated and extracted with diethyl ether (2×). The organic layers were combined, washed with 2N HCl (2×), brine (1×), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give crude 3-(4-heptylcarbamoylmethyl-phenyl)-2,2-dimethyl-propionic acid ethyl ester as an orange oil. The oil was used in the preparation of 3-[4-(2-heptylamino-ethyl)-phenyl]-2,2-dimethyl-propionic acid ethyl ester without further purification. (1.27 g, 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699904B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-4bd769b2ef1a44039cece36e82343f71
출처 메모uspto-grants-2004_03