Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hexane → [1-(6-Benzyloxy-2-naphthylmethyl)-4-phenyl-3-pyrrolyl]methanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Sodium sulfate decahydrate | HCID 62649 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 반응물 | Methyl 1-(6-benzyloxy-2-naphthylmethyl)-4-phenylpyrrole-3-carboxylate | HCID 23024964 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [1-(6-Benzyloxy-2-naphthylmethyl)-4-phenyl-3-pyrrolyl]methanol | HCID 23024834 | 89.1% |
반응 단계
Lithium aluminium hydride (0.258 g) was added to a solution of methyl 1-(6-benzyloxy-2-naphthylmethyl)-4-phenylpyrrole-3-carboxylate (3.04 g) in tetrahydrofuran (30 ml) at 0° C., and the mixture was stirred at room temperature for one hour. Sodium sulfate decahydrate (2.19 g) and hexane (30 ml) were added to the reaction mixture and the mixture was stirred at room temperature for 30 minutes. After the precipitate was removed by filtration, the filtrate was concentrated. The colorless crystals obtained were collected by filtration to yield [1-(6-benzyloxy-2-naphthylmethyl)-4-phenyl-3-pyrrolyl]methanol (2.54 g, yield: 89%). This was recrystallized from ethyl acetate-hexane. Melting point: 116–117° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07179823B1 |
| 출처 데이터셋 | uspto-grants-2007_02 |
| ORD ID | ord-893a5b8d331c4781ae8adea75059963c |
| 출처 메모 | uspto-grants-2007_02 |