Hydrochloric Acid → 3-Phenyloxolan-2-one
反応式
[C:1]1([C:7]([CH2:18][CH2:19][O:20][C:21](=[O:23])C)(C(OCC)=O)C(OCC)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+].Cl>CO>[C:1]1([CH:7]2[CH2:18][CH2:19][O:20][C:21]2=[O:23])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1参加物
5
実験手順
The product of Example 2 (837 g, 2.6M) methanol (1.5 l) and 40% aq. NaOH (1 l, 10M) were heated to reflux for 2 hours. The reaction was then cooled to room temperature and acidified with conc. HCl (1l). The reaction was left as room temperature overnight and then extracted with methyl tert.butyl ether (1 l,500 ml). The extracts were washed with aq. Na2CO3, dried and evaporated to give the title compound(376 g, 89%).
後処理
- temperatureto reflux for 2 hours
- extractionextracted with methyl tert.butyl ether (1 l,500 ml)
- washThe extracts were washed with aq. Na2CO3
- customdried
- customevaporated
出典と根拠
- ORDレコード
- ord-7d238d5a0dac4316a959a22dd1e8cc7f
- 出典データセット
- uspto-grants-1997_05
- 特許番号
- US05629432
反応ノート
読み込み中…