HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Phosphonium, (6-hydroxyhexyl)triphenyl-, bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 6-Bromo-1-hexanol | HCID 77970 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Phosphonium, (6-hydroxyhexyl)triphenyl-, bromide | HCID 2784664 | 93.2% |
Reaction Steps
Into a 5 L, 3 neck round bottom flask fitted with nitrogen inlet, condenser, thermometer, mechanical stirring and nitrogen outlet is added 6-bromo-1-hexanol (500 g, 2.76 mol), triphenylphosphine (768 g, 2.9 mol) and acetonitrile (1800 ml) under nitrogen. The reaction mixture is heated to reflux for 72 hrs. The reaction mixture is cooled to room temperature and transferred into a 5 L beaker. The product is recrystallized from anhydrous ethyl ether (1.5 L) at 10° C. Vacuum filtration of the mixture followed by washing the white crystals with ethyl ether and drying in a vacuum oven at 50° C. for 2 hrs. gives 1140 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133222 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-b8e9983d7c6546aea31c97e12e366129 |
| Source note | uspto-grants-2000_10 |