HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164852Generated: October 30, 2026
Hydrochloric Acid → trans-3-(2,2-Difluoroethenyl)-2,2-dimethylcyclopropanecarboxylic acid
https://huagongshe.com/reaction/2164852
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl trans-3-(2,2-difluoroethenyl)-2,2-dimethylcyclopropanecarboxylate | HCID 70478873 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | trans-3-(2,2-Difluoroethenyl)-2,2-dimethylcyclopropanecarboxylic acid | HCID 67736179 | 92.1% |
Reaction Steps
A stirred solution of ethyl trans-3-(2,2-difluoroethenyl)-2,2-dimethylcyclopropanecarboxylate (10.0 g; 0.049 mole) and 30 ml of an aqueous 10% sodium hydroxide solution in 60 ml of ethanol was heated at reflux for 1.25 hours, then stirred at room temperature for approximately 18 hours. The reaction mixture was heated at 70° C. for an additional 1.5 hours, then cooled to room temperature and poured into 150 ml of an aqueous 5% hydrochloric acid solution. The resultant mixture was extracted with three 50 ml portions of diethyl ether. The extracts were combined, washed twice with water (50 ml) and once with an aqueous saturated sodium chloride solution, then dried over anhydrous magnesium sulfate. The organic solution was filtered, and the filtrate evaporated under reduced pressure to yield 7.95 g of trans-3-(2,2-difluoroethenyl)-2,2-dimethylcyclopropanecarboxylic acid as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04507317 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-138d2ffdcd814db5aeffa18d19ff0450 |
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| Source note | uspto-grants-1985_03 |
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