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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57395생성일: 2026년 10월 26일

Potassium Phosphate, Tribasic → 1-(5-(3-(Trifluoromethyl)phenyl)pyrimidin-2-yl)ethanone

https://huagongshe.com/reaction/57395

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
반응물3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
반응물1-(5-Bromopyrimidin-2-yl)ethan-1-oneHCID 53488064—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물1-(5-(3-(Trifluoromethyl)phenyl)pyrimidin-2-yl)ethanoneHCID 8673017265.5%

반응 단계

A cloudy solution of 1-(5-bromopyrimidin-2-yl)ethanone (300 mg, 1.49 mmol), 3-(trifluoromethyl)phenylboronic acid (567 mg, 2.98 mmol), K3PO4 (950 mg, 4.48 mmol), DavePhos ligand [2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl](59 mg, 0.15 mmol), and Pd(OAc)2 (17 mg, 0.075 mmol) in 6 mL toluene was heated at 100° C. for 1 h. The mixture was cooled to room temperature, and filtered through Celite. Filter cake was rinsed with 30 mL EtOAc. The filtrate was poured into 20 mL water. Layers were separated, and the aqueous was further extracted with EtOAc (20 mL). Combined organics were washed with water (20 mL) and brine (20 mL), dried over Na2SO4, filtered and concentrated directly onto silica gel. Column chromatography (10-100% EtOAc/heptane) gave 0.26 g 1-(5-(3-(trifluoromethyl)phenyl)pyrimidin-2-yl)ethanone as tan solid. MS m/z 267.1 (M+H)+. 1H NMR (400 MHz, CDCl3) δ 9.16 (s, 2H), 7.93-7.69 (m, 4H), 2.87 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434719B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-1308a2f6995e48148fcbb0c8db6844bd
출처 메모uspto-grants-2016_09