HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Triphenylphosphine Oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphine sulfide, triphenyl- | HCID 19758 | — |
| Solvent | Isobutanol | HCID 6560 | — |
| Product | Triphenylphosphine Oxide | HCID 13097 | — |
Reaction Steps
To a mixture of isobutanol (50 ml), triphenylphosphine sulfide (7.0 g) and aqueous 5% sodium hydroxide (50 ml) is bubbled chlorine gas at 15° C. until no appreciable amount of the starting sulfide is detected on thin-layer chromatogram. The reaction mixture is allowed to stand for a while and the organic layer is taken. The layer is washed with water and concentrated to dryness. The residue is triturated with ether to give triphenylphosphine oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04511738 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-2f557de74e6549deac7ee1bd7b7f6940 |
| Source note | uspto-grants-1985_04 |