돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1732989생성일: 2026년 10월 25일

Triethylamine → N-ethyl-N-[3-(methoxycarbonyl)propionyl]-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamine

https://huagongshe.com/reaction/1732989

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Butanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
반응물N-ethyl-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamineHCID 12843078—
용매BenzeneHCID 241—
생성물N-ethyl-N-[3-(methoxycarbonyl)propionyl]-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamineHCID 1284309791.3%

반응 단계

To a mixture of 8.8 g of N-ethyl-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamine, 6.1 g of triethylamine and 80 ml of anhydrous benzene, 7.1 g of 3-(methoxycarbonyl)-propionyl chloride dissolved in 10 ml of anhydrous benzene was added dropwise. After the resulting solution was heated for 2.5 hours at reflux, the solution was allowed to stand overnight at room temperature (about 25° C.). The reaction solution was washed with a 2N-HCl aqueous solution, water, a 2 N-NaOH aqueous solution and water in order, and dried over anhydrous sodium sulfate. Then, the solution was concentrated under reduced pressure to obtain 12.5 g of N-ethyl-N-[3-(methoxycarbonyl)propionyl]-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamine as a pale-yellow oily product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04239903
출처 데이터셋uspto-grants-1980_12
ORD IDord-38d16073cefe451086a1af31cdaf3753
출처 메모uspto-grants-1980_12