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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 485716생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/485716

반응식

참여 물질

역할이름HCID투입량
반응물2,3,4,5,6-Pentafluorobenzyl AlcoholHCID 9923—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물(1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)cyclopropane-carboxylic acidHCID 18599060—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물pentafluorobenzyl (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylateHCID 13171431473%

반응 조건

온도20 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04537897
출처 데이터셋uspto-grants-1985_08
ORD IDord-45c6e0aa1d6c4d56b6c6cbcaf5f003a5
출처 메모uspto-grants-1985_08