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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73338Generated: October 25, 2026

Hydrochloric Acid → Cyano-(4-methoxy-5-methyl-2-nitrophenyl)acetic acid methyl ester

https://huagongshe.com/reaction/73338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl cyanoacetateHCID 7747—
ReactantSodium hydrideHCID 24758—
Reactant1-Fluoro-4-methoxy-5-methyl-2-nitrobenzeneHCID 59850139—
SolventDimethylformamideHCID 6228—
ProductCyano-(4-methoxy-5-methyl-2-nitrophenyl)acetic acid methyl esterHCID 5843726071.7%

Reaction Steps

To a suspension of sodium hydride (0.86 g) in N,N-dimethylformamide (5 mL) was added dropwise a solution of cyano acetic acid methyl ester (0.35 g) in N,N-dimethylformamide (3 mL) under ice cooling and this mixture was stirred for 15 minutes. To this reaction mixture was added dropwise a solution of 1-fluoro-4-methoxy-5-methyl-2-nitrobenzene (0.44 g) under ice cooling and this mixture was stirred at room temperature for 30 minutes, and then stirred at 70° C. overnight. After cooling to ambient temperature, 1 mol/L hydrochloric acid (5 mL) was added to this reaction mixture. This resulting mixture was extracted with ethyl acetate. This organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate) to give the title compound (0.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829040B2
Source datasetuspto-grants-2014_09
ORD IDord-976981bf32554bb7a43ba01cb124ee35
Source noteuspto-grants-2014_09