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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512143생성일: 2026년 10월 26일

Acetic Acid → Cyano-(2-trifluoromethyl-pyrimidin-5-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/512143

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Ethyl cyanoacetateHCID 7764—
반응물Potassium tert-butoxideHCID 23665647—
반응물5-Bromo-2-(trifluoromethyl)pyrimidineHCID 33697963—
촉매palladium(II) acetateHCID 167845—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매1,4-DioxaneHCID 31275—
생성물Cyano-(2-trifluoromethyl-pyrimidin-5-yl)-acetic acid ethyl esterHCID 8671616712.3%

반응 조건

온도70 °C

반응 단계

A mixture of 5-bromo-2-trifluoromethyl-pyrimidine (1.0 g, 4.41 mmol) and cyano-acetic acid ethyl ester (1.0 g, 4.41 mmol) was added into a suspension of t-BuOK (17.64 mL, 17.64 mmol, 1M in THF) in 1,4-dioxane (10 mL) under Ar atmosphere. To the resulting mixture was added a solution of Pd(OAc)2 (10 mg, 44.1 μmol) and dppf (48.9 mg, 88.2 μmol) in 1,4-dioxane (1 mL). The resulting mixture was heated to 70° C. for 1 h. The reaction mixture was adjusted pH to 7˜8 with 1N AcOH and extracted with EtOAc (3×20 ml). The organic layer was dried over Na2SO4 and concentrated. The residue was purified by column chromatography on silica gel (EtOAc:petroleum ether=1:10) to give cyano-(2-trifluoromethyl-pyrimidin-5-yl)-acetic acid ethyl ester (140 mg, yield: 12.3%). 1H NMR (CDCl3 400 Hz): δ9.03 (s, 2H), 4.88 (s, 1H), 4.34 (q, J=7.2 Hz, 2H), 1.35 (t, J=7.2 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102591B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-f1c148c0c1e648f48fd5e92dfbacf50d
출처 메모uspto-grants-2015_08