HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583572Generated: October 31, 2026
Hydrochloric Acid → trans-3-(2,2-Difluoroethenyl)-2,2-dimethylcyclopropanecarboxylic acid
https://huagongshe.com/reaction/1583572
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 10.0 g (0.049 mole) of ethyl trans-3-(2,2-difluoroethenyl)-2,2-dimethylcyclopropanecarboxylate and 30 ml of a 10% aqueous 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 a 5% aqueous 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 a saturated aqueous 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 | US04552892 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-580e5de538c94198bea65c0e63702264 |
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| Source note | uspto-grants-1985_11 |
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