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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088671Generated: November 3, 2026

Hydrochloric Acid → Ethyl[(Z)-2-cyano-1-(2,4-difluorophenyl)ethenyl]carbamate

https://huagongshe.com/reaction/2088671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl CarbonateHCID 7766—
ReactantSodiumHCID 5360545—
Reactant3-Amino-3-(2,4-difluorophenyl)prop-2-enenitrileHCID 66725344—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductEthyl[(Z)-2-cyano-1-(2,4-difluorophenyl)ethenyl]carbamateHCID 58305996—

Reaction Steps

At 40° C., 769 mg (33.44 mmol) of sodium were dissolved in ethanol (41 ml). 4.14 g (22.29 mmol) of 3-amino-3-(2,4-difluorophenyl)prop-2-enonitrile and 5.79 g (49 mmol) of diethyl carbonate were added, and the reaction solution was stirred under reflux for 4 h. 200 ml of ethyl acetate and 150 ml of water were added to the reaction mixture and the pH was adjusted with hydrochloric acid to pH=5. The organic phase was separated off, dried over magnesium sulfate and concentrated on a rotary evaporator. The residue was triturated with diisopropyl ether and the white precipitate was filtered off with suction. More product was obtained by separating the mother liquor by preparative HPLC (Method 11). Drying under high vacuum gave a total of 4.92 g (49% of theory) of the product as a mixture of E and Z isomers which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436003B2
Source datasetuspto-grants-2013_05
ORD IDord-2f4f357b73274f0f9807f875eeafd29f
Source noteuspto-grants-2013_05