Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Aminotetralin → N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Aminotetralin | HCID 34677 | — |
| 반응물 | 2-Naphthyl glycidyl ether | HCID 92995 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine | HCID 19788252 | 53.2% |
반응 단계
A mixture of 1-(2-naphthyloxy)-2,3-epoxypropane (1.95 g), 2-aminotetralin (2.65 g) and ethanol (35 ml) is heated to the reflux temperature for 5 hours. The solvent is then evaporated off and the thus obtained solid residue is crystallized from ethyl acetate (5 ml), recovered by filtration, washed with ethyl acetate and then with ethyl ether, and dried yielding 1.8 g of N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine, as the free base; m.p. 102°-115° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05254595 |
| 출처 데이터셋 | uspto-grants-1993_10 |
| ORD ID | ord-6d61e845ef5d45ed9a722e30b04140de |
| 출처 메모 | uspto-grants-1993_10 |