Nitric Acid → tetrahydro-2H-pyran-3-ol nitrate
反応式
[N+:1]([O-:4])([OH:3])=[O:2].[O:5]1[CH2:10][CH2:9][CH2:8][CH:7](O)[CH2:6]1>C(OC(=O)C)(=O)C>[N+:1]([O:4][CH:7]1[CH2:8][CH2:9][CH2:10][O:5][CH2:6]1)([O-:3])=[O:2]参加物
4
実験手順
In a reaction vessel was placed 50 ml acetic anhydride. While cooling, 14 ml of 90 percent fuming nitric acid was added. Following this, 25 g of tetrahydro-2H-pyran-3-ol was added dropwise at -8° to -10° C. over a one hour period. Stirring was continued for 1.5 hours at -10° C. The mixture was then allowed to warm to room temperature and then poured into an ice-water mixture. The organic phase settled and was separated. The organic phase was diluted with methylene chloride and also washed with aqueous NaHCO3 and dried over MgSO4. The solvent was removed under vacuum leaving 24.04 g of tetrahydro-2H-pyran-3-ol nitrate. The structure was confirmed by IR and NMR analysis.
後処理
- customIn a reaction vessel was placed
- temperatureWhile cooling
- additionwas added dropwise at -8° to -10° C. over a one hour period
- customwas separated
- additionThe organic phase was diluted with methylene chloride
- washalso washed with aqueous NaHCO3
- dry with materialdried over MgSO4
- customThe solvent was removed under vacuum
出典と根拠
- ORDレコード
- ord-98cd71fc582d42829c733a3fb4a2c434
- 出典データセット
- uspto-grants-1983_09
- 特許番号
- US04405333
反応ノート
読み込み中…