反応式
[CH2:1]1[O:3][C@@H:2]1[CH2:4][OH:5].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F:25][C:26]1[CH:27]=[CH:28][C:29]([N+:33]([O-:35])=[O:34])=[C:30](O)[CH:31]=1.CCOC(/N=N/C(OCC)=O)=O>C1COCC1>[F:25][C:26]1[CH:31]=[CH:30][C:29]([N+:33]([O-:35])=[O:34])=[C:28]([CH:27]=1)[O:5][CH2:4][C@@H:2]1[CH2:1][O:3]1参加物
実験手順
In a flask was added (R)-glycidol (0.994 g, 13.4 mmole) and triphenylphosphine (3.52 g, 13.4 mmole) and THF (20 ml, dried over molecular sieves), and 5-fluoro-2-nitrophenol (2.10 g, 13.4 mmole). The mixture was stirred until a homogeneous solution was obtained. The solution was cooled in an ice bath and diethylazodicarboxylate (DEAD, 2.11 ml, 13.4 mmole) was added dropwise over a few minutes. After completed addition, the flask was allowed to reach room temperature and stirred for an additional 2 hours. The solvent was removed in vaccuo and to the residue was added chloroform (5-10 ml). The precipitate (PPh3O) was removed by filtration and the solid was washed with an additional amount of chloroform (5-10 ml). The filtrate was added to a flash column (SiO2, Heptane:Ethyl acetate 4:1), and purified to give 2.02 g (71%) of the sub-title compound as a crystalline material after concentration of pure fractions.
後処理
- customwas obtained
- temperatureThe solution was cooled in an ice bath
- additionaddition
- customto reach room temperature
- stirringstirred for an additional 2 hours
- customThe solvent was removed in vaccuo and to the residue
- additionwas added chloroform (5-10 ml)
- customThe precipitate (PPh3O) was removed by filtration
- washthe solid was washed with an additional amount of chloroform (5-10 ml)
- additionThe filtrate was added to a flash column (SiO2, Heptane:Ethyl acetate 4:1)
- custompurified
出典と根拠
- ORDレコード
- ord-5791f1f45ed74a45a12eb55b525798bc
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07388020B2
関連ノート
読み込み中…