戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 485716作成日:2026年10月27日

2,3,4,5,6-Pentafluorobenzyl Alcohol → pentafluorobenzyl (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylate

https://huagongshe.com/reaction/485716

反応式

関与物質

役割名称HCID仕込み量
反応物2,3,4,5,6-Pentafluorobenzyl AlcoholHCID 9923—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物(1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)cyclopropane-carboxylic acidHCID 18599060—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物pentafluorobenzyl (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylateHCID 13171431473%

反応条件

温度20 °C

反応手順

A solution of 4.12 g of dicyclohexylcarbodiimide in 40 ml of methylene chloride was added at 0° C. to a mixture of 3 g of (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylic acid, 30 ml of methylene chloride, 3.96 g of pentafluorobenzyl alcohol and 100 mg of 4-dimethylaminopyridine and the mixture was stirred at 20° C. for 16 hours and was filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with a 9-1 hexane-ethyl acetate mixture yielded 4.78 g of pentafluorobenzyl (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylate with a specific rotation of [α]D20 =-23° (c=0.5% in chloroform).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04537897
出典データセットuspto-grants-1985_08
ORD IDord-45c6e0aa1d6c4d56b6c6cbcaf5f003a5
出典メモuspto-grants-1985_08