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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573563Generated: October 25, 2026

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

https://huagongshe.com/reaction/573563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantEthyl cyanoacetateHCID 7764—
Reactant3-MethoxyacetophenoneHCID 11460—
ReactantHexamethyldisilazaneHCID 13838—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductEthyl 2-cyano-3-[3-(methyloxy)phenyl]-2-butenoateHCID 411500286.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029545B2
Source datasetuspto-grants-2015_05
ORD IDord-02851e9ff45a4b3ca21cb5998be3404f
Source noteuspto-grants-2015_05