戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 598240作成日:2026年10月26日

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

https://huagongshe.com/reaction/598240

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Acryloyl chlorideHCID 13140—
反応物Ethyl 3-amino-4,4,4-trifluoro-2-butenoateHCID 136209—
溶媒TolueneHCID 1140—
溶媒HeptaneHCID 8900—
生成物Ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carboxylateHCID 277439235%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07897621B2
出典データセットuspto-grants-2011_03
ORD IDord-54a8f275ab634a6e8849c5ba7621e217
出典メモuspto-grants-2011_03