Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Hexamethylphosphorous triamide | HCID 15355 | — |
| Reactant | HCID 20553527 | HCID 20553527 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 88745964 | HCID 88745964 | 52.8% |
Reaction Steps
Tri(dimethylamino)phosphine (40 mmol) was added with stirring at -20° C. to a solution of 1-(2-formyl-3,3-dimethylcyclopropyl)-3-oxo-2-butyl acetate (14.2 mmol) and carbon tetrachloride (40 mmol) in diethyl ether (160 ml) kept under nitrogen. Then, the temperature of the mixture was allowed to rise to 20° C. Water (50 ml) was added, the mixture was stirred for 5 minutes and, after settling, the organic phase was isolated. The organic phase was washed with two 50-ml portions of water. The washed organic phase was dried over anhydrous magnesium sulphate and the solvent was evaporated from the dried solution to leave a residue (2.2 g) containing 1-[2-(2,2-dichlorovinyl)-3,3-dimethylcyclopropyl]-3-oxo-2-butyl acetate (100% (1R,cis), yield 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04314072 |
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| Source dataset | uspto-grants-1982_02 |
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| ORD ID | ord-b5c50bb1d6544f0d9ad78ce6c0eaf388 |
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| Source note | uspto-grants-1982_02 |
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