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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474238Generated: November 3, 2026

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

https://huagongshe.com/reaction/1474238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-(4-cyano-3-methoxyphenyl)acetateHCID 66643843—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(4-cyano-3-methoxyphenyl)propanoateHCID 66643920—

Reaction Steps

To a suspension solution of NaH (0.18 g, 4.6 mmol, 60% dispersion in mineral oil) in THF (50 mL) at 0° C. under N2 atm was added a solution of ethyl (4-cyano-3-methoxyphenyl)acetate (1.0 g, 4.6 mmol) in THF (10 mL) drop-wise and the mixture was stirred for 30 min at the same temperature. The mixture was then allowed to warm to ambient temperature. The mixture was then allowed to cool back to 0° C. Methyl iodide (0.28 mL, 4.6 mmol) was added and the reaction mixture was stirred for 1 h. The reaction mixture was acidified with 1 M hydrochloric acid and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane/EtOAc 15/1) to give ethyl 2-(4-cyano-3-methoxyphenyl)propanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-9e51ee72357c479486c04a8c81b0f56b
Source noteuspto-grants-2015_04