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HRID 247694作成日:2026年10月24日

Dicyclohexylcarbodiimide → HCID 178444551、化合物

https://huagongshe.com/ja/reaction/247694

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物4-EthoxyphenolHCID 12150—
反応物HCID 178444555HCID 178444555—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物HCID 178444551HCID 17844455183.5%

反応手順

A mixture of 520 mg of trans-4-(4-pentenyl)cyclohexanecarboxylic acid, 439.4 mg of p-ethoxyphenol, 765.5 mg of dicyclohexylcarbodiimide and 45 mg of 4-(dimethylamino)pyridine were dissolved in 80 ml of methylene chloride and the solution was stirred at room temperature for 20 hours. Subsequently, the reaction mixture was diluted with diethyl ether, the precipitated urea was filtered off and the filtrate was concentrated. The residue was taken up in hexane and the solution was washed with dilute hydrochloric acid, sodium hydrogen carbonate solution and water. The aqueous phases were back-extracted twice with hexane. The organic phases were dried over magnesium sulphate and evaporated. Low-pressure chromatography of the resulting residue on silica gel with ethyl acetate/petroleum ether (vol. 3:97) gave an 0.7 g (83%) of trans-4-(4-pentenyl)cyclohexanecarboxylic acid p-ethoxyphenyl ester. After recrystallization from 3 ml of methanol there were finally obtained 455 mg of product in the form of colourless crystals; m.p. (C-N) 32.7° C., cl.p. (N-I) 57.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04709030
出典データセットuspto-grants-1987_11
ORD IDord-88d42fa00ec645d7b222c81884225647
出典メモuspto-grants-1987_11