Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 21423413 | HCID 21423413 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21423425 | HCID 21423425 | 63.9% |
Reaction Steps
A solution of 1-chloro-3-propoxyacetone (8.5 g.) and triphenylphosphine (15.6 g.) in chloroform (20 ml.) was saturated with nitrogen and heated at reflux under nitrogen overnight. An excess of dry diethyl ether was added, and then the solvents were decanted from the gum that separated. The remaining solvent was removed in vacuo to give crude 2-oxo-3-propoxypropyltriphenylphosphonium chloride (14.9 g.). This was stirred vigorously with a solution of sodium carbonate (14.6 g.) in water (146 ml.) for 24 hours. The solution was extracted with diethyl ether and the ethereal extracts dried over sodium sulphate. The solvent was removed by evaporation, and the residue was triturated with petroleum to give propoxyacetylmethylenetriphenylphosphorane (6.3 g.), a sticky solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04036872 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-8ee2b51beeee460e92995f6e01c74bc5 |
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| Source note | uspto-grants-1977_07 |
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