Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-ethyl-N-[3-(methoxycarbonyl)propionyl]-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Butanoic acid, 4-chloro-4-oxo-, methyl ester | HCID 73888 | — |
| 반응물 | N-ethyl-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamine | HCID 12843078 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | N-ethyl-N-[3-(methoxycarbonyl)propionyl]-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamine | HCID 12843097 | 91.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04239903 |
| 출처 데이터셋 | uspto-grants-1980_12 |
| ORD ID | ord-38d16073cefe451086a1af31cdaf3753 |
| 출처 메모 | uspto-grants-1980_12 |