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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598240생성일: 2026년 10월 25일

Hydrochloric Acid → Ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate

https://huagongshe.com/reaction/598240

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Acryloyl chlorideHCID 13140—
반응물Ethyl 3-amino-4,4,4-trifluoro-2-butenoateHCID 136209—
용매TolueneHCID 1140—
용매HeptaneHCID 8900—
생성물Ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carboxylateHCID 277439235%

반응 단계

To 3-amino-4,4,4-trifluoro-2-butenoic acid ethyl ester (529 mL, 3.47 mol) was added acryloylchloride (600 mL, 6.95 mol) dropwise over a period of 15 min. The suspension was stirred at RT for 1 h. The temperature was slowly raised with stirring to 80° C. (HCl gas evolution) and maintained at 80° C. for 5 h. Stirring continued overnight at 40° C. The mixture was cooled, diluted with toluene (2 L) and n-heptane (2 L) to precipitate the product and stirred for another 15 min at room temperature. The product was isoloated by filtration, the filter cake was washed with toluene/n-heptane (1:2; 4×100 mL) and dried in vacuo at 40° C. for 5 h. This procedure yielded the title compound (286 g, 35%) as a white solid, MS (ISP) 236.1 (M−H)−. Concentration of the mother liquor and addition of toluene/n-heptane (1:10) yielded a second crop of 29.8 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897621B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-54a8f275ab634a6e8849c5ba7621e217
출처 메모uspto-grants-2011_03