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HRID 2085625作成日:2026年10月27日

Cyclohexane, (ethenyloxy)- → HCID 12994198、化合物

https://huagongshe.com/reaction/2085625

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclohexane, (ethenyloxy)-HCID 75129—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物2-Methylpropyl-(R)-2-hydroxypropanoateHCID 10486989—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 12994198HCID 1299419899.5%

反応手順

A catalytic amount of pyridinium para-toluenesulfonate was added to 29.2 g (0.2 mole) of isobutyl (R)-(+)-lactate and 28.0 g (0.22 mole) of cyclohexyl vinyl ether. The resulting mixture was stirred at room temperature for 4 hours to give rise to a reaction. Thereto was added 100 ml of ethyl acetate, followed by washing with 100 ml of a saturated aqueous sodium hydrogen carbonate solution, 40 ml of water and 40 ml of a saturated aqueous sodium chloride solution in this order. The washed material was dried over anhydrous sodium sulfate and then subjected to vacuum distillation to remove the solvent, whereby was obtained 54.2 g (yield: 99.4%) of an oily title compound (diastereomixture).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06720463B1
出典データセットuspto-grants-2004_04
ORD IDord-f3ffd66015e743289eaaf4ea9e62d370
出典メモuspto-grants-2004_04