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HRID 8223생성일: 2026년 10월 26일

Citric Acid → 2-(4-Fluoro-phenyl)-3-oxo-3-(6-trifluoromethyl-pyridin-2-yl)-propionitrile

https://huagongshe.com/reaction/8223

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Benzeneacetonitrile, 4-fluoro-HCID 68016—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물6-trifluoromethyl-pyridine-2-carbothioic acid S-(4-chloro-phenyl) esterHCID 4156106—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물2-(4-Fluoro-phenyl)-3-oxo-3-(6-trifluoromethyl-pyridin-2-yl)-propionitrileHCID 2199264166%

반응 단계

A solution of 4-fluorophenylacetonitrile (0.12 mL, 1.0 mmol) in dry tetrahydrofuran (2 mL) is treated dropwise with potassium bis(trimethylsilyl)amide (0.5 M toluene, 3.0 mL, 1.5 mmol) at 0° C. under an atmosphere of nitrogen. The mixture is stirred 10 min then 6-trifluoromethyl-pyridine-2-carbothioic acid S-(4-chloro-phenyl) ester is added all at once. The mixture is allowed to warn to room temperature then warmed to reflux for 10 min, at which time the reaction is complete by TLC (methylene chloride). The mixture is allowed to cool then poured into 10% citric acid and extracted into methylene chloride. The methylene chloride solution is dried over magnesium sulfate and concentrated in vacuo. The residue is purified on a silica gel cartridge prepared with hexane then eluted with methylene chloride to yield 204 mg (66%) 2-(4-fluoro-phenyl)-3-oxo-3-(6-trifluoromethyl-pyridin-2-yl)-propionitrile. MS ES− m/z 307 (M−1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087626B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-93bcccec9d1e4801a4fde7f976f24c31
출처 메모uspto-grants-2006_08