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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253704생성일: 2026년 10월 26일

Methyl pivaloylacetate → 6-tert-Butyl-2-(2-trifluoromethyl-phenyl)-3H-pyrimidin-4-one

https://huagongshe.com/reaction/253704

반응식

참여 물질

역할이름HCID투입량
반응물Methyl pivaloylacetateHCID 99597—
반응물Sodium ethoxideHCID 2723922—
반응물2-TrifluoromethylbenzamidineHCID 3266509—
용매EthanolHCID 702—
생성물6-tert-Butyl-2-(2-trifluoromethyl-phenyl)-3H-pyrimidin-4-oneHCID 13615719032.4%

반응 단계

A mixture of 2-trifluoromethylbenzamidine (1.12 g, 5 mmol), sodium ethoxide (1.02 g, 15 mmol) and 4,4-dimethyl-3-oxo-pentanoic acid methyl ester (0.80 mL, 5 mmol) in ethanol (50 mL) and was heated at reflux for 16 hours. The reaction was cooled, concentrated, diluted with water and acidified with 2 N hydrochloric acid. This solution was extracted with ethyl acetate, dried over sodium sulfate and concentrated. Purification by flash chromatography [SiO2, methanol:dichloromethane (2:98)] provided the title compound (0.48 g, 32% yield) as a yellow solid; 1H-NMR (500 MHz, DMSO-d6) δ 12.8 (br s, 1H), 7.89 (d, J=7.5 Hz, 1H), 7.78 (m, 2H), 7.71 (d, J=7.4 Hz, 1H), 6.24 (s, 1H), 1.20 (s, 9H) ppm; LC-MS 297.03 (M+H); Rt (Method A) 3.30 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872129B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-eea643965fc04e5f98dae4cbfd3e22de
출처 메모uspto-grants-2011_01