HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine dibromide → HCID 18177453, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine dibromide | HCID 70579 | — |
| Reactant | HCID 18177470 | HCID 18177470 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18177453 | HCID 18177453 | — |
Reaction Steps
4.79 g (8.95 mmol) of dibromotriphenylphosphorane are added to a solution of 2.4 g (8.95 mmol) of the alcohol obtained in Step A in 80 ml of acetonitrile. After 15 minutes of stirring under argon, the solvent is evaporated in vacuo; the residue obtained is then taken up in an ether/hexane mixture (1/1). The solid formed is filtered off; the filtrate is then concentrated under reduced pressure to yield the brominated compound of the title in the form of a chestnut-brown syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313160B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-5799f30f2b5645c3a0a76923e1b7811c |
| Source note | uspto-grants-2001_11 |