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HRID 1907677생성일: 2026년 10월 26일

Hydrochloric Acid → Diethyl 2-(3-(trifluoromethyl)pyridin-2-yl)malonate

https://huagongshe.com/reaction/1907677

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl MalonateHCID 7761—
반응물Sodium hydrideHCID 24758—
반응물2-Chloro-3-(trifluoromethyl)pyridineHCID 589833—
촉매Cupric ChlorideHCID 24014—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물Diethyl 2-(3-(trifluoromethyl)pyridin-2-yl)malonateHCID 5795021327.4%

반응 단계

8.73 g of sodium hydride (55% oil dispersion) was suspended in 100 ml of 1,4-dioxane. Into this, 32.03 g of diethyl malonate was added dropwise over a period of about 1 hour at 60° C. under a nitrogen atmosphere. The mixture was stirred further for 0.5 hours at the same temperature, then, 8.26 g of copper chloride (I) was added to the mixture. Thereafter, into the mixture, a solution prepared by dissolving 15.00 g of 2-chloro-3-(trifluoromethyl)pyridine in 50 ml of 1,4-dioxane at 80° C. was dropped. The mixture was stirred for 16 hours under reflux with heating. The reaction mixture was allowed to cool to room temperature, and to the reaction mixture was added 15 ml of concentrated hydrochloric acid. To the mixture were added water and ethyl acetate, and the mixture was filtrated through celite. The filtrate was liquid-separated. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. 51.14 g of the resultant residue was subjected to silica gel column chromatography, to obtain 6.90 g of diethyl (3-trifluoromethyl-2-pyridyl)malonate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598176B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-c664465c17ad4d7dbb08de2c0cb69feb
출처 메모uspto-grants-2013_12