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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | 1,3-Pentadiene, 1,1-dichloro-4-methyl- | HCID 108746 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Catalyst | Hexadecyltrimethylammonium Bromide | HCID 5974 | — |
| Catalyst | Triethylmethylammonium chloride | HCID 82326 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Butyl Acetate | HCID 31272 | — |
| Product | Ethyl 1-cyano-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04284582 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-81838b762819421ba96dfa284e7b5a28 |
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| Source note | uspto-grants-1981_08 |
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