反応式
Br[CH2:2][CH2:3][OH:4].C(=O)([O-])[O-].[K+].[K+].[OH:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=[O:17])=[CH:14][CH:13]=1>CC#N>[OH:4][CH2:3][CH2:2][O:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=[O:17])=[CH:14][CH:13]=1参加物
5
実験手順
2-Bromoethanol (5.8 mL) and potassium carbonate (11.3 g) were successively added to a solution of 4-hydroxybenzaldehyde (5.0 g) in MeCN (100 mL). The resulting mixture was stirred and heated at reflux for 3 days under argon. The reaction mixture was cooled to RT and partitioned between EtOAc (100 mL) and 1M aqueous NaOH solution (100 mL). The organic layer was washed with brine (100 mL). The aqueous layers were combined and extracted with EtOAc (50 mL). The organic layers were combined, dried over sodium sulphate, filtered and evaporated in vacuo to give the subtitled compound as a yellow oil. Yield 6.4 g.
後処理
- temperatureheated
- temperatureat reflux for 3 days under argon
- custompartitioned between EtOAc (100 mL) and 1M aqueous NaOH solution (100 mL)
- washThe organic layer was washed with brine (100 mL)
- extractionextracted with EtOAc (50 mL)
- dry with materialdried over sodium sulphate
- filtrationfiltered
- customevaporated in vacuo
出典と根拠
- ORDレコード
- ord-908502f4afa8461491c445c15679a5e0
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08629271B2
関連ノート
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