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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526432Generated: October 28, 2026

Hydrochloric Acid → Ethyl 2-(4-cyano-2-methoxyphenyl)-3-(dimethylamino)acrylate

https://huagongshe.com/reaction/526432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
ReactantDimethylformamide diethylacetalHCID 70913—
ReactantEthyl 2-(4-cyano-2-methoxyphenyl)acetateHCID 117600541—
ReactantTert-butyl 2-(4-cyano-2 methoxyphenyl)acetateHCID 117601441—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(4-cyano-2-methoxyphenyl)-3-(dimethylamino)acrylateHCID 11760103074%

Reaction Conditions

Temperature100 °C

Reaction Steps

Combined tert-butyl 2-(4-cyano-2-methoxyphenyl)acetate (549 mg, 2.218 mmol) and 4N HCl in dioxane (0.277 mL, 1.109 mmol) in ethanol (7.4 mL) and stirred for 16 hours at 60° C. The reaction was concentrated by rotary evaporation and then combined with ethyl 2-(4-cyano-2-methoxyphenyl)acetate (0.486 g, 2.217 mmol) and 1,1-diethoxy-N,N-dimethylmethanamine (1.9 mL, 11.08 mmol) in DMF (4.43 mL) and stirred for 16 hours at 100° C. The reaction mixture was diluted with 200 mL EtOAc and washed twice with 200 mL water. Organic layer was dried with sodium sulfate and concentrated to give a residue which was purified on a 60 g NH silica gel column eluting with hexanes and EtOAc to give the title compound (405 mg, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345713B2
Source datasetuspto-grants-2016_05
ORD IDord-8e16190dd5b04168948c0b4c0bd1e4ca
Source noteuspto-grants-2016_05