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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1636447생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1636447

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
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—
용매TetrahydrofuranHCID 8028—
생성물(2,3,5,6-tetrafluoro-4-methylphenyl)methyl(1R)-trans-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylateHCID 1158098787%

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06034128
출처 데이터셋uspto-grants-2000_03
ORD IDord-1b830a87e7ee4673bc868bb63b5d3002
출처 메모uspto-grants-2000_03