反応式
[CH3:1][C:2]1([C:8]([OH:10])=[O:9])[CH2:7][CH2:6][CH:5]=[CH:4][CH2:3]1.OS(O)(=O)=O>C(Cl)(Cl)Cl>[CH3:1][C:2]12[C:8](=[O:10])[O:9][CH:4]([CH2:5][CH2:6][CH2:7]1)[CH2:3]2参加物
反応条件
- 温度
- 0 °C
実験手順
A solution of 1-methyl-3-cyclohexenecarboxylic acid (47 g) in chloroform (200 ml) was cooled to -5° C. Then, a mixture of conc. H2SO4 (100 ml) and chloroform (100 ml) was added. After stirring at 0° C. for 15 minutes, the mixture was poured onto ice (500 g) and extracted with chloroform. The chloroform layer was washed in sequence with water, saturated aqueous sodium hydrogen carbonate solution and water, and dried (MgSO4), and the chloroform was distilled off. The residual oily substance was subjected to column chromatography using silica gel (500 g) and eluted with ether-hexane (1:3 v/v). From the first eluate fractions, crystals of 1-methylcyclohexane-1,3-carbolactone (28.0 g, 59.6% yield) were recovered and recrystallized from hexane. m.p. 37°-38° C.
後処理
- additionwas added
- additionthe mixture was poured onto ice (500 g)
- extractionextracted with chloroform
- washThe chloroform layer was washed in sequence with water, saturated aqueous sodium hydrogen carbonate solution and water
- dry with materialdried (MgSO4)
- distillationthe chloroform was distilled off
- washeluted with ether-hexane (1:3 v/v)
出典と根拠
- ORDレコード
- ord-fd567031eb5c458cabb3aa63998416eb
- 出典データセット
- uspto-grants-1984_07
- 特許番号
- US04461902
関連ノート
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