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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616196생성일: 2026년 10월 24일

Ammonia → 2-Phenyl-2-[4-(1-methyl-1,2,3,4-tetrahydro-4-quinolyl)-phenoxy]-propionitrile

https://huagongshe.com/ko/reaction/616196

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Dimethyl SulfateHCID 6497—
반응물2-Phenyl-2-[4-(1-methyl-1,2,3,4-tetrahydro-4-quinolyl)-phenoxy]-acetonitrileHCID 20371431—
촉매Ferric nitrateHCID 25251—
생성물2-Phenyl-2-[4-(1-methyl-1,2,3,4-tetrahydro-4-quinolyl)-phenoxy]-propionitrileHCID 20371430—

반응 단계

At -40°, 50 mg. of iron (III) nitrate and then, under agitation, 2.3 g. of Na are dissolved in 100 ml. of liquid ammonia. After two hours of agitation, 3.54 g. of 2-phenyl-2-[4-(1-methyl-1,2,3,4-tetrahydro-4-quinolyl)-phenoxy]-acetonitrile is added thereto, the mixture stirred for 30 minutes, and then 19.2 ml. of dimethyl sulfate is added dropwise within one hour. The mixture is further agitated overnight at -35° and then combined dropwise with another 10 ml. of dimethyl sulfate. After the ammonia has been evaporated, the residue is combined with water and extracted with ether. The crude 2-phenyl-2-[4-(1-methyl-1,2,3,4-tetrahydro-4-quinolyl)-phenoxy]-propionitrile obtained after the evaporation of the ether is refluxed for 40 hours with 3 g. of KOH in 30 ml. of ethanol and 3 ml. of water. The mixture is concentrated by evaporation, mixed with water, extracted with ether, hydrochloric acid is added to pH 5, and the acid Ih is thus produced.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04072754
출처 데이터셋uspto-grants-1978_02
ORD IDord-250b17d88f0f46d59e9a692e1469af56
출처 메모uspto-grants-1978_02