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HRID 2232621作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/2232621

反応式

関与物質

役割名称HCID仕込み量
反応物(Diethylamino)sulfur trifluorideHCID 123472—
反応物2-(5-Phenyl-1-hydroxypentyl)-2-oxiranecarboxylic acid methyl esterHCID 14348902—
溶媒DichloromethaneHCID 6344—
生成物2-(1-Fluoro-5-phenylpentyl)-2-oxiranecarboxylic acid methyl esterHCID 14348905—

反応条件

温度-78 °C

反応手順

To a solution of 2.44 g (15 mmol; 2.01 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 (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) γ1750 cm-1 ; NMR (CDCl3) δ1.40-1.96 (6H, m), 2.64 (2H, t, J=8 Hz), 3.07 (1H, dd, J=4, 6 Hz), 3.15 (1H, d, J=6 Hz), 3.79 (3H, s), 5.14 (1H, ddd, JHF =49 Hz, J=10, 3 Hz), 7.21 (2H, d, J=8 Hz) and 7.31 (2H, d, J=8 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04788304
出典データセットuspto-grants-1988_11
ORD IDord-eaa72b054dc540aaa2f6325685222f05
出典メモuspto-grants-1988_11