HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-(1,3-Diphenyl-1-propoxy)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triphenylphosphane dibromide | HCID 12890784 | — |
| Reactant | 4-(1,3-Diphenyl-1-propoxy)benzyl alcohol | HCID 54118543 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(1,3-Diphenyl-1-propoxy)benzyl bromide | HCID 53849933 | — |
Reaction Steps
To an ice cold solution of 6-5 (1.19 g, 6.0 mmol) in acetonitrile (15 ml) was added pyridine (0.76 g, 9.6 mmol) and then triphenylphosphine dibromide (3.29 g, 7.8 mmol). The mixture was stirred at ice bath temperature for 1/4 hr under N2 and at ambient temperature for 1 &3/4 hrs and then was filtered. Concentration of the filtrate in vacuo gave a crude oil. The pure product 6-6 was obtained after three silica gel chromatographic separations.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05872138 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-e3011c2937014a46978d9d92fb3b23c3 |
| Source note | uspto-grants-1999_02 |