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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894491Generated: October 26, 2026

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

https://huagongshe.com/reaction/894491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl cyanoacetateHCID 7764—
ReactantCalcium CarbonateHCID 10112—
ReactantBromineHCID 24408—
ReactantChlorineHCID 24526—
Reactant1,3-Pentadiene, 1,1-dichloro-4-methyl-HCID 108746—
ReactantPotassium BromideHCID 253877—
ReactantCalcium ChlorideHCID 5284359—
ReactantSodium HypochloriteHCID 23665760—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
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-4-methylpenta-1,3-diene (30.2 parts) cupric chloride (2.68 parts), calcium carbonate (40 parts), calcium chloride and potassium bromide as indicated in the table below, is heated in water in the presence of a phase transfer catalyst (either cetyl trimethyl ammonium bromide (CTMAB) or methyl triethyl ammonium chloride (MTEAC)]]. Sodium hypochlorite solution, bromine or chlorine are then added at a uniform rate to the mixture at an elevated temperature. Heating is continued for a further period. After cooling the reaction mixture, the suspension is diluted with butyl acetate (100 parts by volume). Concentrated hydrochloric acid (50 parts by volume) diluted with water (100 parts) is slowly added, the mixture is stirred for about 30 minutes and then filtered to remove extraneous matter. The butyl acetate layer is separated and washed with water (4×50 parts). The butyl acetate is removed by distillation under reduced pressure to yield crude ethyl 1-cyano-3-(2',2'-dichlorovinyl)-2,2-dimethylcyclopropane -1-carboxylate. Details of the reaction conditions are given in the table below, together with the yield, strength and composition of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284582
Source datasetuspto-grants-1981_08
ORD IDord-81838b762819421ba96dfa284e7b5a28
Source noteuspto-grants-1981_08