Toluene → Methyl 4-(5-cyano-7-isopropenyl-1,3-benzoxazol-2-yl)benzoate
反応式
Br[C:2]1[C:10]2[O:9][C:8]([C:11]3[CH:19]=[CH:18][C:14]([C:15]([O-:17])=[O:16])=[CH:13][CH:12]=3)=[N:7][C:6]=2[CH:5]=[C:4]([C:20]#[N:21])[CH:3]=1.[C:22]1(C)[CH:27]=CC=C[CH:23]=1.[C:29](=O)([O-])[O-].[Na+].[Na+].C(B(O)O)=CC(=C)C>C(O)C.O>[C:20]([C:4]1[CH:3]=[C:2]([C:22]([CH3:27])=[CH2:23])[C:10]2[O:9][C:8]([C:11]3[CH:19]=[CH:18][C:14]([C:15]([O:17][CH3:29])=[O:16])=[CH:13][CH:12]=3)=[N:7][C:6]=2[CH:5]=1)#[N:21]参加物
反応条件
- 温度
- 91 °C
実験手順
To a 5-l, 3-neck round-bottom flask fitted with a stirring paddle, a condenser blanketed with nitrogen, and a thermocouple, was added 4-(7-bromo-5-cyano-1,3-benzoxazol-2-yl)benzoate (55.5 g, INTERMEDIATE 1) toluene (2 l), water (375 ml), ethanol (150 ml), 2M aqueous sodium carbonate (250 ml), and isoprenylboronic acid (83.4 g, INTERMEDIATE 3). The mixture was purged with nitrogen three times and then tetrakis(triphenylphosphine)palladium(0) (9.1 g) was added, and the mixture was purged three times with nitrogen. The mixture was heated to reflux (91° C.) and stirred at this temperature overnight. The mixture was then cooled to 20° C. and the product was filtered, washed with water, dried, and transferred to a 3-l round-bottom flask and rinsed with toluene (1 l). Residual solvent was removed in vacuo. Mass spectrum (ESI) 319.1 (M+1).
後処理
- customThe mixture was purged with nitrogen three times
- additiontetrakis(triphenylphosphine)palladium(0) (9.1 g) was added
- customthe mixture was purged three times with nitrogen
- temperatureThe mixture was heated
- temperatureThe mixture was then cooled to 20° C.
- filtrationthe product was filtered
- washwashed with water
- customdried
- customtransferred to a 3-l round-bottom flask
- washrinsed with toluene (1 l)
- customResidual solvent was removed in vacuo
出典と根拠
- ORDレコード
- ord-d9d045efc71246a7886de28a8eee081e
- 出典データセット
- uspto-grants-2013_05
- 特許番号
- US08445480B2
反応ノート
読み込み中…