Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Boron trifluoride → 1-Naphthol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Boron trifluoride | HCID 6356 | — |
| 반응물 | 1-Naphthol | HCID 7005 | — |
| 반응물 | beta-D-Ribofuranose, 1-acetate 2,3,5-tribenzoate | HCID 81455 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-Naphthol | HCID 7005 | — |
| 생성물 | HCID 18731516 | HCID 18731516 | — |
반응 단계
A solution 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose (500 mg, 0.99 mmol), α-naphthol (428 mg, 3.00 mmol) and boron trifluoride diethyletherate (141 mg, 0.99 mmol. 125 μl) in dry dichloromethane (5 ml) was stirred at room temperature under argon for 16 hours. The mixture was worked up as for Stage 1 of Example 1 and purified by flash chromatography on silica gel (eluting with dichloromethane:hexanes, 3:2) to afford the title compound contaminated with α-naphthol. The latter was removed by dissolving the residue in ethyl acetate and washing with 10% aqueous sodium hydroxide solution, which after conventional processing, gave 136 mg, 23% of product as a yellow gum.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06379911B2 |
| 출처 데이터셋 | uspto-grants-2002_04 |
| ORD ID | ord-d29c5ad3b72a470cbe102ea3c53a1c86 |
| 출처 메모 | uspto-grants-2002_04 |