反応式
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]([CH:11]=[CH:12][CH:13](O)[CH3:14])[CH:2]=1.C(O)(=O)CC.[C:21](OCC)([O:26]CC)([O:23][CH2:24][CH3:25])[CH3:22]>[Cl-].[Na+].O>[CH2:24]([O:23][C:21](=[O:26])[CH2:22][CH:11]([C:3]1[CH:2]=[N:1][C:10]2[C:5]([CH:4]=1)=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:12]=[CH:13][CH3:14])[CH3:25]参加物
5
実験手順
A solution of the allylic alcohol 22-2 (1.2 g, 6.1 mmol) in triethyl orthoacetate (50 mL) was treated with propionic acid (0.022 mL, 0.31 mmol) and refluxed for 2 h. The cooled mixture was treated with a solution of 1:1 sat. brine/1N HCl (150 mL), then extracted with CH2Cl2 (3×125 mL). The pooled organic extracts were washed with sat. NaHCO3, dried, filtered and evaporated. Chromatography on silica gel (EtOAc) afforded 22-3 as a yellow glass.
後処理
- temperaturerefluxed for 2 h
- extractionextracted with CH2Cl2 (3×125 mL)
- washThe pooled organic extracts were washed with sat. NaHCO3
- customdried
- filtrationfiltered
- customevaporated
出典と根拠
- ORDレコード
- ord-c6a3ecf53028441689f01256bbf4ddad
- 出典データセット
- uspto-grants-2000_04
- 特許番号
- US06048861
関連ノート
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