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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238391생성일: 2026년 10월 26일

Triphenylphosphine → 1-Methyl-5-{2-[4-(trifluoromethyl)phenoxy]ethyl}-1H-pyrazole

https://huagongshe.com/reaction/238391

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물4-(Trifluoromethyl)phenolHCID 67874—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물2-(1-methyl-1H-pyrazol-5-yl)ethan-1-olHCID 21832419—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-Methyl-5-{2-[4-(trifluoromethyl)phenoxy]ethyl}-1H-pyrazoleHCID 8955870354.6%

반응 단계

A mixture of 2-(1-methyl-1H-pyrazol-5-yl)ethanol (1.00 g), 4-hydroxybenzotrifluoride (2.57 g), 1.9 M diisopropyl azodicarboxylate (6.26 mL, toluene solution), triphenylphosphine (3.12 g) and tetrahydrofuran (50 mL) was stirred at a room temperature for 2 days. Thereafter, water was added to the reaction solution, and the obtained mixture was then extracted with ethyl acetate. The organic layer was washed with water, and was then dried over anhydrous sodium sulfate, followed by vacuum concentration. The residue was purified by column chromatography (silica gel cartridge, hexane/ethyl acetate=90:10 to 55:45), so as to obtain the title compound (1.17 g) in the form of a light yellow oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642626B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-ad54ccf442e04ba5aae94821068c84c9
출처 메모uspto-grants-2014_02