Ethanol → HCID 21544827、化合物
反応式
[C:1]([C:4]1[C:21]([OH:22])=[CH:20][CH:19]=[CH:18][C:5]=1[O:6][CH2:7][CH:8]([OH:17])[CH2:9][O:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)(=[O:3])[CH3:2].[O-:23][CH2:24][CH3:25].[Na+].[Na].C([OH:30])C>C(OCC)(=O)C(OCC)=O.C1C=CC=CC=1.CCOCC>[C:24]([C:25]1[O:22][C:21]2[C:4]([C:1](=[O:3])[CH:2]=1)=[C:5]([O:6][CH2:7][CH:8]([OH:17])[CH2:9][O:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH:18]=[CH:19][CH:20]=2)([OH:30])=[O:23]参加物
実験手順
A solution of 1-(2-acetyl-3-hydroxyphenoxy)-2-hydroxy-3-phenoxypropane (12.08 g) in diethyl oxalate (30 ml) was added to a suspension of sodium ethoxide, prepared from sodium (6.0 g) and ethanol (60 ml), in benzene (100 ml). The mixture was heated under reflux for 1.5 hours, cooled and poured into ether. The precipitated yellow solid was collected, washed with ether and dried. The solid was then added to a mixture of glacial acetic acid (80 ml) and concentrated hydrochloric acid (30 ml) and heated under reflux for 1 hour. After cooling, the reaction mixture was poured with stirring into cold water (1 L). The precipitated gum was washed with water by decantation and solidified by trituration with acetic acid. Recrystallization from acetic acid gave 1-(2-carboxychromon-5-yloxy)-2-hydroxy-3-phenoxypropane (7.0 g) as a white powder, m.p. 88°-90° C.
後処理
- temperatureThe mixture was heated
- temperatureunder reflux for 1.5 hours
- temperaturecooled
- customThe precipitated yellow solid was collected
- washwashed with ether
- customdried
- additionThe solid was then added to a mixture of glacial acetic acid (80 ml) and concentrated hydrochloric acid (30 ml)
- temperatureheated
- temperatureunder reflux for 1 hour
- temperatureAfter cooling
- additionthe reaction mixture was poured
- washThe precipitated gum was washed with water by decantation
- customRecrystallization from acetic acid
出典と根拠
- ORDレコード
- ord-060a4ae06dd04aba8035bbcf9683f65f
- 出典データセット
- uspto-grants-1976_04
- 特許番号
- US03953604
反応ノート
読み込み中…