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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894495Generated: October 25, 2026

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

https://huagongshe.com/reaction/894495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl cyanoacetateHCID 7764—
ReactantMagnesium CarbonateHCID 11029—
ReactantCalciumHCID 5460341—
Reactant1,1-Dichloro-3,4-dibromo-4-methylpent-1-eneHCID 20574281—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
CatalystCopperHCID 23978—
CatalystTriethylmethylammonium chlorideHCID 82326—
SolventWaterHCID 962—
SolventButyl AcetateHCID 31272—
ProductEthyl 1-cyano-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylateHCID 12898169—

Reaction Steps

A mixture of ethyl cyanoacetate (24.88 parts), 1,1-dichloro-3,4-dibromo-4-methylpent-1-ene (62.2 parts), calcium or magnesium carbonate and metal chloride is heated in water (100 parts) in the presence of a phase transfer catalyst (either cetyl trimethyl ammonium bromide (CTMAB) or methyl triethyl ammonium chloride (MTEAC)]] and a copper salt as catalyst. The reaction mass is cooled to room temperature, n-butyl acetate (100 parts by volume) water (100 parts) and hydrochloric acid (100 parts by volume) are added and the mixture is stirred for 30 minutes, filtered from extraneous matter and the filtrates separated. The butyl acetate layer is washed with water (4×100 parts) and evaporated under reduced pressure to remove the butyl acetate and yield the crude ethyl 1-cyano-3-(2',2'-dichlorovinyl)-2,2-dimethyl-cyclopropane-1-carboxylate. The yield, strength and composition of the product is given in the following table, together with other details.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284582
Source datasetuspto-grants-1981_08
ORD IDord-1f98ea6235da407b987a205ab0fdcc38
Source noteuspto-grants-1981_08