Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)-
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Pyrrolidine | HCID 31268 | — |
| 반응물 | 6-Chloro-2-tetralone | HCID 4456139 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)- | HCID 10444008 | — |
반응 단계
1155 g (6.4 mol) of 6-chloro-3,4-dihydro-2(1H)-naphthalenone were dissolved in 5 l of toluene, 500 g (7.0 mol) of pyrrolidine and subsequently a solution of 26 g (0.14 mol) of p-toluenesulphonic acid in toluene were added dropwise thereto and the mixture was boiled under reflux. When about 120 ml of water had separated, 4 l of toluene were distilled off and the mixture was left to cool slowly. A solid crystallized out. Filtration and washing with acetone gave 1-(6-chloro-3,4-dihydro-2-naphthyl)pyrrolidine of melting point 117°-118°. Concentration of the mother liquor, suspension of the residue in ether, filtration and washing with acetone gave a further portion of the above product of melting point 117°-118°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04749791 |
| 출처 데이터셋 | uspto-grants-1988_06 |
| ORD ID | ord-9f02db5146114d8b94e41f4ce3ed4995 |
| 출처 메모 | uspto-grants-1988_06 |