反応式
[OH:1][CH2:2][C:3]1[O:4][CH:5]=[CH:6][C:7](=[O:10])[C:8]=1[OH:9].[CH2:11](Br)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[OH:1][CH2:2][C:3]1[O:4][CH:5]=[CH:6][C:7](=[O:10])[C:8]=1[O:9][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1参加物
3
実験手順
The title compound was prepared by the method outlined for 2-hydroxymethyl-3-benzyloxy-6-methyl-pyran-4(1B)-one, using 7.1 g (50 mmol, 1 eq.) of 2-hydroxymethyl-3-hydroxy-pyran-4(1 H)-one and 9.5 g benzyl bromide (55 mmol, 1.1 eq.) to yield the crude product as an organe oil. Further purification by column chromatography on silica gel (eluant: 10% CH3OH/90% CHCl3) furnished the pure product (9.4 g, 81%) as a bright yellow oil. (Looker and Clifton (1986).
後処理
- customto yield the crude product as an organe oil
出典と根拠
- ORDレコード
- ord-271da8747afa47808b6e219f5988638b
- 出典データセット
- uspto-grants-2002_01
- 特許番号
- US06335353B1
関連ノート
読み込み中…