Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzyl Bromide → (2S,3S,4S,5R,6R)-benzyl 3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzyl Bromide | HCID 7498 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | beta-D-glucopyranuronic acid | HCID 441478 | — |
| 반응물 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Isopropanol methylene chloride | HCID 21966342 | — |
| 생성물 | (2S,3S,4S,5R,6R)-benzyl 3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylate | HCID 58148857 | 65% |
반응 단계
To a solution of (2S,3S,4S,5R,6R)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylic acid (1 g, 5.15 mmol) and TBAF in THF (6.18 mL, 6.18 mmol) in DMF (7 mL) was slowly added (bromomethyl)benzene (0.925 g, 5.41 mmol) at 0° C. The clear solution was warmed up to room temperature slowly and let it stir for 17 hours. TLC indicated the reaction was completed (20% iPrOH/CH2Cl2). The solvent was removed and the reaction residue was purified by silica gel chromatography with 10-20% iPrOH/CH2Cl2 to provide the desired product as a colorless oil (950 mg, 65%). LCMS: m/e 283.31 (M−H)−, 2.55 min (method 10).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08846647B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-936e74c96b654b12b1c7a5f7ca94e20b |
| 출처 메모 | uspto-grants-2014_09 |