反応式
[O:1]=[CH:2][C@H:3]([C@H:5]([C@@H:7]([CH2:9][OH:10])[OH:8])[OH:6])[OH:4].[CH2:11](O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C(OCC)C>[O:1]([CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C@H:2]1[O:10][CH2:9][C@@H:7]([OH:8])[C@H:5]([OH:6])[C@@H:3]1[OH:4]参加物
4
反応条件
- 温度
- -5 °C
実験手順
A mixture of D-lyxose (10 g, 66.6 mmol) and benzyl alcohol (50 ml) was cooled to -5° C. and hydrogen chloride was bubbled through it for 3 to 5 hours while monitoring the reaction on tlc (ethyl acetate-ethyl alcohol 7:1). To this reaction mixture diethyl ether (100 ml) was added with stirring and the mixture was allowed to stand at 5° C. for 12 hours. The crystals were filtered, washed with ether and air dried to give 4 (14.1 g, 88.1%).
後処理
- customhydrogen chloride was bubbled through it for 3 to 5 hours
- customthe reaction on tlc (ethyl acetate-ethyl alcohol 7:1)
- filtrationThe crystals were filtered
- washwashed with ether and air
- customdried
出典と根拠
- ORDレコード
- ord-f9b7839603514c9d8d055fe2a413cb99
- 出典データセット
- uspto-grants-1998_06
- 特許番号
- US05773239
関連ノート
読み込み中…