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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 573563생성일: 2026년 10월 25일

Dichloromethane → Ethyl 2-cyano-3-[3-(methyloxy)phenyl]-2-butenoate

https://huagongshe.com/reaction/573563

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Ethyl cyanoacetateHCID 7764—
반응물3-MethoxyacetophenoneHCID 11460—
반응물HexamethyldisilazaneHCID 13838—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물Ethyl 2-cyano-3-[3-(methyloxy)phenyl]-2-butenoateHCID 411500286.3%

반응 단계

Hexamethyldisilazane (17.45 mL, 83 mmol) was added dropwise to acetic acid (38.1 mL, 666 mmol) (caution exothermic, maintain below 70° C.) stirred under an atmosphere of nitrogen. The resulting mixture was added to a solution of 1-[3-(methyloxy)phenyl]ethanone (9.14 mL, 66.6 mmol) and ethyl cyanoacetate (11.75 mL, 110 mmol) in acetic acid (16 mL), which was then stirred at 70° C. for 18 h. The mixture was then allowed to cool to RT and DCM (350 mL) and water (125 mL) were added. The organic layer was then separated and washed with additional water (125 mL) and dried with anhydrous MgSO4, filtered and evaporated to dryness. The residue was purified on silica, eluting with a gradient of 0-30% ethyl acetate in isohexane and further purified on silica, eluting with a gradient of 0-25% ethyl acetate in isohexane, to afford the title compound (14.1 g). LCMS (A) m/z: 246 [M+1]+, Rt 1.28 min (basic).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029545B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-02851e9ff45a4b3ca21cb5998be3404f
출처 메모uspto-grants-2015_05