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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894488Generated: October 25, 2026

Hydrochloric Acid → Ethyl 1-cyano-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylate

https://huagongshe.com/reaction/894488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantCalcium CarbonateHCID 10112—
ReactantEthyl 2-bromo-2-cyanoacetateHCID 14469—
Reactant1,3-Pentadiene, 1,1-dichloro-4-methyl-HCID 108746—
ReactantCalciumHCID 5460341—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventButyl AcetateHCID 31272—
ProductEthyl 1-cyano-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylateHCID 12898169—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1,1-dichloro-4-methylpenta-1,3-diene (30.2 parts), ethyl bromocyanoacetate (38.4 parts), calcium carbonate (20 parts), copper catalyst, phase transfer catalyst and calcium or sodium chloride (each as indicated in the table below) and water (100 parts) is heated at 80° C. and held at 80° C. for 6 hours. The reaction mixture is cooled and stirred with water (100 parts), butyl acetate (100 parts by volume) and concentrated hydrochloric acid (100 parts by volume). The mixture is filtered and the residue is washed with butyl acetate (2×20 parts by volume). The filtrate and washes are combined and the butyl acetate layer is separated and washed with water (4×50 parts). The crude ethyl-1-cyano-3-(2',2'-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylate is isolated by removal of the butyl acetate under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284582
Source datasetuspto-grants-1981_08
ORD IDord-db4f54f5210949e58fe9a53847bdc973
Source noteuspto-grants-1981_08