반응식
[Na].[OH:2][C:3]1[C:4](=[O:11])[CH:5]=[C:6]([CH2:9][OH:10])[O:7][CH:8]=1.[CH2:12](Br)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>CO>[OH:10][CH2:9][C:6]1[O:7][CH:8]=[C:3]([O:2][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:4](=[O:11])[CH:5]=1참가 물질
5
반응 조건
- 온도
- 30 °C
실험 절차
69 g (3 mmol) of sodium were dissolved in 5 l of methanol. Subsequently 425.3 g (3 mol) of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one was added and stirred at 30° C. until a clear solution was obtained. 595 g (3.5 mol) of benzyl bromide was then added and stirred for 1 hour under reflux. The warm, dark colored solution was poured into 15 l of ice water. The product crystallized immediately. The crystals were collected and washed first with 8 l of water and then twice with 2.5 l of ether. The product was left to stand overnight and finally dried at 50° C. for 16 hours. Yield: 646 g.
후처리
- customwas obtained
- stirringstirred for 1 hour
- temperatureunder reflux
- customThe product crystallized immediately
- customThe crystals were collected
- washwashed first with 8 l of water
- waitThe product was left
- customfinally dried at 50° C. for 16 hours
출처 및 근거
- ORD 기록
- ord-da936a24b5e443619348b1d75c279850
- 출처 데이터셋
- uspto-grants-1988_02
- 특허 번호
- US04723002
연결된 노트
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