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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392361생성일: 2026년 10월 25일

Ethyl Acetate → HCID 22662796, 화합물

https://huagongshe.com/reaction/392361

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물18-Crown-6HCID 28557—
반응물6-Chloropyrazine-2-carbonitrileHCID 81303—
반응물Potassium FluorideHCID 522689—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매AcetonitrileHCID 6342—
생성물HCID 22662796HCID 2266279649.3%

반응 단계

In a mixture of 140 ml of acetonitrile and 280 ml of toluene were suspended 58 g of potassium fluoride (spray-dried) and 8.7 g f 18-crown-6-ether. After heating the suspension under reflux for one hour in an atmosphere of nitrogen gas, the acetonitrile and toluene were distilled off under atmospheric pressure. The residue thus obtained was suspended in 280 mL of acetonitrile, 23 g of 6-chloro-2-pyrazinecarbonitrile synthesized according to the method described in Acta Poloniae Pharmaceutica, Vol. 33, Pages 153-161 (1976) was added, and the mixture thus obtained was heated under reflux for one hour in an atmosphere of nitrogen. The reaction mixture was cooled to room temperature, 280 mL of ethyl acetate and 280 mL of water were added, and the organic layer was separated. The organic layer thus obtained was washed successively with water and saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was distilled off under a reduce pressure. The residue was purified by silica gel column chromatography [eluent: n-hexane:ethyl acetate=10:1] to obtain 10 g of 6-fluoro-2-pyrazinecarbonitrile as a white-colored solid product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06800629B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-5c6ed00921bc476eb4b71e438687f8ad
출처 메모uspto-grants-2004_10