反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[C:7]([C:12]1[C:13]([CH3:18])=[N:14][O:15][C:16]=1[CH3:17])(OCC)=[O:8].S([O-])([O-])(=O)=O.[Na+].[Na+]>CCOCC>[CH3:18][C:13]1[C:12]([CH2:7][OH:8])=[C:16]([CH3:17])[O:15][N:14]=1参加物
実験手順
A suspension of 100 g. (2.63 moles) of lithium aluminum hydride in 2.5 liters of anhydrous ether was stirred under nitrogen as a solution of 272 g. (1.61 mole) of the 4-carboethoxy-3,5-dimethylisoxazole prepared in Example 1 above in 400 ml. of anhydrous ether was added at such a rate as to maintain a gentle reflux. The suspension was stirred at room temperature under nitrogen overnight, during which time an extremely gummy green-gray mass formed in the bottom of the flask. The mixture was cooled in an ice bath and hydrolyzed with saturated aqueous sodium sulfate solution. Anhydrous sodium sulfate was added to dry the ether solution. The salts were removed by filtration and washed carefully with ether and chloroform. Solvent removal from the filtrates, finally at 50°/0.1 mm., gave a white crystalline mass. This was triturated with hot ether and then cooled. Filtration gave 3,5-dimethyl-4-hydroxymethyl-isoxazole as white prisms, m.p. 76.5°-77.5°. Concentration of the mother liquors gave a second crop of prisms, m.p. 76.5°-78°.
後処理
- additionA suspension of 100 g
- temperatureto maintain a gentle reflux
- customformed in the bottom of the flask
- dry with materialto dry the ether solution
- customThe salts were removed by filtration
- washwashed carefully with ether and chloroform
- customSolvent removal from the filtrates
- customfinally at 50°
- custom, gave a white crystalline mass
- customThis was triturated with hot ether
- temperaturecooled
- filtrationFiltration
出典と根拠
- ORDレコード
- ord-c9b4ad6a2efd4e94804cebff9296db1e
- 出典データセット
- uspto-grants-1977_08
- 特許番号
- US04044004
関連ノート
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