Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, ethyl ester | HCID 101094 | — |
| Reactant | Sodium dodecylbenzene sulphonate | HCID 57371080 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Permethric acid | HCID 91658 | 85% |
Reaction Steps
27.9 g. of 2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropane-1-carboxylic acid ethyl ester (purity: 85%, cis) trans ratio: 40:60/, 6 g. of a 25% aqueous sodium hydroxide solution and 0.01 g. of sodium dodecylbenzene sulfonate are stirred at a temperature of 80° C. for 30 minutes. Hydrolysis is then continued with a further 5 g. portion of sodium hydroxide solution for 60 minutes and subsequently with an additional 5 g. portion of a sodium hydroxide solution for 150 minutes. The mixture is diluted with 30 ml. of water, cooled to 20° C. and the unreacted compounds are dissolved in 10 ml. of hexane. To the aqueous phase 80 ml. of hexane are added and the organic acid is set free by adding 12 g. of a 36% aqueous hydrochloric acid solution with stirring. The hexane solution is separated, decolored with 0.5 g. of activated carbon, filtered, 35 ml. of the solvent are distilled off and the residue is crystallized at -5° C. for 48 hours. The crystals are filtered off and dried. 17.8 g. (85%) of 2,2-dimethyl-3-(2,2-dichlorovinyl)-cyclopropane-1-carboxylic acid are obtained. Cis/trans ratio: 40:60.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04419524 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-086dc95a8ace45d49905e55fd882d7b4 |
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| Source note | uspto-grants-1983_12 |
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