HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphine sulfide, triphenyl- → Triphenylphosphine Oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphine sulfide, triphenyl- | HCID 19758 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Triphenylphosphine Oxide | HCID 13097 | — |
Reaction Steps
To a mixture of triphenylphosphine sulfide (0.3 g) and ethyl acetate (10 ml) is added thionyl chloride (0.16 ml) at room temperature, and the mixture is stirred for 2 hours at the same temperature. The reaction mixture is shaken with aqueous 6% sodium hydrogen carbonate (20 ml) and the resulting mass is stirred for another 2 hours. The organic layer which forms on standing for a while is taken, washed with water, filtered to remove a solid mass and concentrated to dryness. The residue is crystallized from ether to give triphenylphosphine oxide (0.26 g). m.p. 155°-156° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04511738 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-3db6450ea7624374b1ac11a52734c717 |
| Source note | uspto-grants-1985_04 |