HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412461Generated: October 31, 2026
Diethyl (trichloromethyl)phosphonate → Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, ethyl ester
https://huagongshe.com/reaction/2412461
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (trichloromethyl)phosphonate | HCID 70085 | — |
| Reactant | Ethyl 3-formyl-2,2-dimethylcyclopropane-1-carboxylate | HCID 566079 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, ethyl ester | HCID 101094 | 60% |
Reaction Steps
A mixture of 25.5 g (0.1 mole) of trichloromethanephosphonic acid diethyl ester and 17.2 g (0.1 mole) of 3-formyl-2,2-dimethyl-cyclopropane-1-carboxylic acid ethyl ester was added dropwise to 9.6 g of activated magnesium filings in 100 ml of dimethylformamide in a manner such that the reaction temperature did not exceed 60° C. When the exothermic reaction had ended, the reaction mixture was allowed to cool to room temperature. It was then filtered. 200 ml of water were added to the filtrate; this solution was extracted twice with 100 ml of methylene chloride each time. The combined methylene chloride extracts were dried over sodium sulphate and filtered. The filtrate was distilled. 3-(2,2-Dichloro-vinyl)-2,2-dimethyl-cyclopropane-1-carboxylic acid ethyl ester was obtained in a yield of 60% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04492800 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-c0039e41640d4216b9cc860ae1672ec7 |
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| Source note | uspto-grants-1985_01 |
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