反応式
[CH3:1][Mg]Cl.[NH2:4][C:5]1[C:14](C)=[CH:13][CH:12]=[CH:11][C:6]=1[C:7](OC)=O.CC[O:18][CH2:19][CH3:20]>C1COCC1>[NH2:4][C:5]1[C:6]([CH3:7])=[CH:11][CH:12]=[CH:13][C:14]=1[C:19]([CH3:20])([CH3:1])[OH:18]参加物
実験手順
130 ml of a 3 M solution of methyl magnesium chloride in 130 ml of THF was added drop-by-drop to a stirred solution of 11 g of 49A in 70 ml of dry ether at 0°-5° C. in a nitrogen atmosphere. The resulting mixture was allowed to warm to room temperature and stirred at reflux (40° C.) for 5 hours and held overnight at room temperature. The mixture then was quenched in a mixture of 48 g of ammonium chloride and 350 g of ice. 30 ml of 3 N hydrochloric acid was added, the solvents were evaporated, and the residue was extracted with ether. The extract phase was washed with water, then brine, dried (K2CO3), filtered and stripped of solvent. The residue was recrystallized from hexane to give (2-amino-3-methylphenyl)dimethylcarbinol (49B), as colorless needles, m.p.: 78°-79° C.
後処理
- temperatureat reflux (40° C.) for 5 hours
- customThe mixture then was quenched in a mixture of 48 g of ammonium chloride and 350 g of ice
- addition30 ml of 3 N hydrochloric acid was added
- customthe solvents were evaporated
- extractionthe residue was extracted with ether
- washThe extract phase was washed with water
- dry with materialbrine, dried (K2CO3)
- filtrationfiltered
- customThe residue was recrystallized from hexane
出典と根拠
- ORDレコード
- ord-9c4b2bda46d44deea438d113df671bec
- 出典データセット
- uspto-grants-1987_10
- 特許番号
- US04699651
関連ノート
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