反応式
C([O-])(=O)C.[NH4+].C([BH3-])#[N:7].[Na+].[Cl:10][C:11]1[CH:21]=[CH:20][C:14]([O:15][CH2:16][C:17](=O)[CH3:18])=[C:13]([CH3:22])[CH:12]=1>CO>[Cl:10][C:11]1[CH:21]=[CH:20][C:14]([O:15][CH2:16][CH:17]([NH2:7])[CH3:18])=[C:13]([CH3:22])[CH:12]=1参加物
実験手順
120 g of ammonium acetate and 9.8 g of sodium cyanoborohydride were added to a solution containing 31 g of (4-chloro-2-methylphenoxy)acetone dissolved in 700 ml of methanol, and the resultant mixture was stirred for 20 hours at room temperature. After the reaction mixture was concentrated under reduced pressure, 180 ml of concentrated hydrochloric acid and 100 ml of water were added to the residue. The whole mixture was stirred for 1 hour, and then 300 ml of diethyl ether was added thereto. The aqueous layer was alkalified using a 5% aqueous solution of sodium hydroxide, and then extracted with 500 ml of ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. A fraction possessing a low boiling point was removed from the obtained oily products to afford 25 g (yield 81 %) of the desired product.
後処理
- concentrationAfter the reaction mixture was concentrated under reduced pressure, 180 ml of concentrated hydrochloric acid and 100 ml of water
- additionwere added to the residue
- addition300 ml of diethyl ether was added
- extractionextracted with 500 ml of ethyl acetate
- washThe organic layer was washed with water
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- customwas removed from the obtained oily products
出典と根拠
- ORDレコード
- ord-af2d6d23050641d68165ae7f72c039be
- 出典データセット
- uspto-grants-1998_09
- 特許番号
- US05811424
関連ノート
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