Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Ethyl 3-oxohexanoate | HCID 238498 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54188657 | HCID 54188657 | — |
Reaction Steps
280 g of phosphorus pentachloride are added in portions over the course of 2 hours to a solution of 200 g of 3-oxo-hexanoic acid ethyl ester in 20 ml of absolute benzene whilst stirring at 20° C. 200 ml of water are then added dropwise with intense cooling so that the temperature never rises above 0° C. The mixture is stirred for a further 12 hours at 0° C. The organic phase is then separated off, washed with twice 100 ml of ice-cold 2 N sodium hydroxide solution and with twice 100 ml of water, dried over sodium sulphate and evaporated in vacuo. Fractional distillation of the evaporation residue gives, in the fraction boiling at 98°-102° C (20 mm), crude 3-chloro-2-hexenoic acid ethyl ester, which is used direct for further conversion.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04035413 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-1b922dc6c3b64d5eaea1c107598994e3 |
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| Source note | uspto-grants-1977_07 |
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