Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → HCID 15868597, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 1-Chloro-4-morpholin-4-yl-2-naphthol | HCID 609692 | — |
| 반응물 | 1-(4-Methoxyphenyl)-1-phenylprop-2-yn-1-ol | HCID 3694873 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | HCID 15868597 | HCID 15868597 | 16.1% |
반응 단계
0.91 g of 1-chloro-4-morpholino-2-naphthol are allowed to react with 0.95 g of 1-(p-methoxyphenyl)-1-phenyl-2-propyn-1-ol in 30 ml of THF under reflux for 4 hours in the presence of 0.72 g of p-toluene sulfonic acid. The solution is then neutralized with 30 ml of 1N sodium hydroxide and then extracted twice with 30 ml of toluene. The organic phases are evaporated and then the photochrome is separated by chromatography on an alumina column in eluting with a mixture of ethyl acetate/diisopropyl ether (10/90). 250 mg of 3-(p-methoxyphenyl)-3-phenyl-6-morpholino-[3H]-naphtho-[2,1-b]pyran (compound II) are thus obtained. Its structure is confirmed by 1H NMR spectroscopy.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06291561B1 |
| 출처 데이터셋 | uspto-grants-2001_09 |
| ORD ID | ord-73ef1642fb0741b8b5be34d34d6f5756 |
| 출처 메모 | uspto-grants-2001_09 |