HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Phenoxyacetylmethyltriphenylphosphonium Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Chloro-3-phenoxypropan-2-one | HCID 11622456 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Phenoxyacetylmethyltriphenylphosphonium Chloride | HCID 20516787 | 62.9% |
Reaction Steps
A solution of 1-chloro-3-phenoxyacetone (6.8 g.) and triphenylphosphine (12 g.) in chloroform (16 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-phenoxypropyltriphenylphosphonium chloride (10.35 g.). This was stirred vigorously with a solution of sodium carbonate (18 g.) in water (180 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 to give phenoxyacetylmethylenetriphenylphosphorane (5.3 g.), a sticky solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04088695 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-cd4334fe59b44f9595ffa1a47a517bdc |
| Source note | uspto-grants-1978_05 |