N-bromobutanimide → 3-Acetyl-4-hydroxy-6-bromomethylpyran-2-one
反応式
[C:1]([C:4]1[C:5](=[O:12])[O:6][C:7]([CH3:11])=[CH:8][C:9]=1[OH:10])(=[O:3])[CH3:2].[Br:13]N1C(=O)CCC1=O>ClCCl>[C:1]([C:4]1[C:5](=[O:12])[O:6][C:7]([CH2:11][Br:13])=[CH:8][C:9]=1[OH:10])(=[O:3])[CH3:2]参加物
4
実験手順
A mixture of 3-acetyl-4-hydroxy-6-methylpyran-2-one (52 parts), N-bromosuccinimide (54 parts) and dichloromethane (1060 parts) were stirred at 20°-25° C. for about 4-5 hours under exposure to UV light. The dichloromethane solution was washed with water (2×500 cm3) to remove the succinimide, dried over magnesium sulphate, filtered and the solvent removed at 40° C./20 mm to leave 3-acetyl-6-bromomethyl-4-hydroxypyran-2-one (70 parts, 47%).
後処理
- washThe dichloromethane solution was washed with water (2×500 cm3)
- customto remove the succinimide
- dry with materialdried over magnesium sulphate
- filtrationfiltered
- customthe solvent removed at 40° C./20 mm
出典と根拠
- ORDレコード
- ord-7940590eee534e9bb31d2a8fb743e35c
- 出典データセット
- uspto-grants-1995_08
- 特許番号
- US05443970
反応ノート
読み込み中…