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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1976307생성일: 2026년 10월 26일

Pyridine → (2,3,5,6-tetrafluoro-4-methylphenyl)methyl(1R)-trans-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1976307

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물TetrahydrofuranHCID 8028—
반응물4-Methyl-2,3,5,6-tetrafluorobenzyl alcoholHCID 2734209—
반응물(1R,3R)-2,2-Dimethyl-3-(2-methyl-1-propen-1-yl)cyclopropanecarbonyl chlorideHCID 10867076—
용매Ethyl acetate hexaneHCID 21226206—
생성물(2,3,5,6-tetrafluoro-4-methylphenyl)methyl(1R)-trans-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylateHCID 1158098787.1%

반응 단계

To a mixture solution of 1.78 g of (2,3,5,6-tetrafluoro-4-methylphenyl)methanol, 0.87 g of pyridine and 20 ml of tetrahydrofuran, 2.06 g of (1R)-trans-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic chloride was added under ice-cooling and the mixture was stirred for 8 hours at room temperature. The reaction mixture was poured into about 100 ml of ice-water and extracted with each 100 ml of ethyl acetate twice. The combined ethyl acetate was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a crude product, which was subjected to silica gel column chromatography (eluent: hexane/ethyl acetate=20/1) to give 2.75 g of (2,3,5,6-tetrafluoro-4-methylphenyl)methyl(1R)-trans-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate (yield 87%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06225495B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-1fb30dc999774aaf95acac4f309849c9
출처 메모uspto-grants-2001_05