反応式
[CH3:1][C:2]1([CH3:13])[O:6][C:5](=[O:7])[CH:4]=[C:3]1N1CCCC1.C[OH:15]>Cl>[OH:15][C:3]1[C:2]([CH3:13])([CH3:1])[O:6][C:5](=[O:7])[CH:4]=1参加物
4
反応条件
- 温度
- 88 °C
実験手順
A suspension of 5,5-dimethyl-4-pyrrolidin-1-ylfuran-2(5H)-one (535 mg) in a mixture of MeOH (2 mL) and 5M HCl (8 mL) was heated at 88° C. for 2 hours. The mixture was cooled to room temp., extracted with CHCl3 (10×15 mL), combined, dried over Na2SO4, and evaporated to dryness to give 4-hydroxy-5,5-dimethyl-5H-furan-2-one as light brown solid. Yield: 359 mg, 95%.
後処理
- temperatureThe mixture was cooled to room temp.
- extractionextracted with CHCl3 (10×15 mL)
- dry with materialdried over Na2SO4
- customevaporated to dryness
出典と根拠
- ORDレコード
- ord-5f75305b2f2e40abb74ffdea41f99db7
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08865682B2
関連ノート
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