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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2232655생성일: 2026년 10월 24일

(Diethylamino)sulfur trifluoride → 2-(1-Fluoro-5-phenylpentyl)-2-oxiranecarboxylic acid methyl ester

https://huagongshe.com/ko/reaction/2232655

반응식

참여 물질

역할이름HCID투입량
반응물(Diethylamino)sulfur trifluorideHCID 123472—
반응물2-(5-Phenyl-1-hydroxypentyl)-2-oxiranecarboxylic acid methyl esterHCID 14348902—
용매DichloromethaneHCID 6344—
생성물2-(1-Fluoro-5-phenylpentyl)-2-oxiranecarboxylic acid methyl esterHCID 1434890558.8%

반응 조건

온도-78 °C

반응 단계

To a solution of 2.44 g (15 mmol; 2.0 ml) of diethylaminosulfur trifluoride in 50 ml of methylene chloride cooled to -78° C. under a nitrogen atmosphere is added dropwise a solution of 2.00 g (7.6 mmol) of 2-[1-hydroxy-5-phenylpentyl]-2-oxiranecarboxylic acid methyl ester (isomer A) in 50 ml of methylene chloride over 30 minutes. The mixture is stirred at -78° C. for 90 minutes and then is allowed to come to room temperature. The mixture is stirred at room temperature for 1.5 hours, is quenched with a saturated aqueous solution of sodium bicarbonate and is extracted with ethyl ether. The combined ethereal extracts are dried over magnesium sulfate, filtered and rotoevaporated. The resulting oil is purified chromatographically (silica gel; hexane:ethyl acetate (9:1)) to give 1.19 g of the title compound (Rf 0.54 in hexane:ethyl ether (3:2)): IR (neat) γ 1750 cm-1 ; NMR (CDCl3) δ 1.40-1.96 (6H, m), 2.64 (2H, t, J=8 Hz), 3.07 (1H, dd, J=4, 6 Hz), 3.15 (1H, d, J=6 Hz), 3.15 (1H, d, J=6 Hz), 3.79 (3H, s), 5.14 (1H, ddd, JHF =48 Hz, J=10, 3 Hz), 7.21 (2H, d, J=8 Hz) and 7.31 (2H, d, J=8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04788306
출처 데이터셋uspto-grants-1988_11
ORD IDord-e8cb0699909c4e7da290e5f59a089625
출처 메모uspto-grants-1988_11