HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Phenoxyacetylmethyltriphenylphosphonium Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Chloro-3-phenoxypropan-2-one | HCID 11622456 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Phenoxyacetylmethyltriphenylphosphonium Chloride | HCID 20516787 | — |
Reaction Steps
1-Chloro-3-phenoxyacetone (13 g, 0.07 mole) dissolved in 20 ml chloroform was mixed with a solution of triphenylphosphine (19.7 g, 1 eq) in 30 ml chloroform at room temperature. The mixture was swirled for 5 minutes and benzene (20 ml) was added. A white crystalline compound appeared when most of the solvents had been evaporated. The product was collected by suction and washed with benzene. Second and third crops were collected by evaporation of the washings. The total yield was 23 g (73%); sublimation without melting at 90°; ir (KBr, cm-1) 3450-3280, 2770, 1720, 1595, 1585, 1485, 1435, 1220, 1110, 1030; nmr (DCCl3, ppm) 8.20-6.80 (m, 22H), 5.30 (br, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04361514 |
| Source dataset | uspto-grants-1982_11 |
| ORD ID | ord-10c4aa3e386641168dec94f2a230de63 |
| Source note | uspto-grants-1982_11 |