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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1042745생성일: 2026년 10월 26일

Ethyl Acetate → 5-Bromo-2-chloro-4-(2-ethoxyphenoxy)pyrimidine

https://huagongshe.com/reaction/1042745

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물2-EthoxyphenolHCID 66755—
반응물5-Bromo-2,4-dichloropyrimidineHCID 289973—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
생성물5-Bromo-2-chloro-4-(2-ethoxyphenoxy)pyrimidineHCID 79076541—

반응 단계

To a suspension of NaH (0.42 g 60% in mineral oil, 10.5 mmol) in DMF (8.0 mL) was slowly added 2-ethoxylphenol (1.34 g, 9.7 mmol) in MeCN (4.0 mL) at 0° C. under N2. After the addition, the reaction mixture was allowed to warm up to room temperature for 0.5 hour. 5-bromo-2,4-dichloropyrimidine (2.0 g, 8.8 mmol) in MeCN (16.0 mL) was slowly added and then the resulting reaction mixture was stirred at room temperature for 24 hour. EtOAc (120 mL) was added and washed with NaOH (30 mL, 0.5N) and brine (25×2 mL). The organic layer was dried with MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (10% to 30% EtOAc in Hexanes, gradient elution) to provide the 5-bromo-2-chloro-4-(2-ethoxyphenoxy)pyrimidine. MS m/z=330 [M+1]+. Calc'd for: C12H10BrClN2O2: 329

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08557996B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-ea489643db744541870091d3137221ac
출처 메모uspto-grants-2013_10