HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-(p-Tert.butyl-phenyl)-2-methyl-allyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | 3-(4-tert-Butylphenyl)-2-methylprop-2-en-1-ol | HCID 54381367 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 3-(p-Tert.butyl-phenyl)-2-methyl-allyl bromide | HCID 57204175 | — |
Reaction Steps
73.2 g of 3-(p-tert.butyl-phenyl)-2-methyl-allyl alcohol nd 8.6 ml of pyridine in 700 ml of n-pentane are cooled down to -5° C. At this temperature there are added dropwise while stirring over a period of 2 hours 15.2 ml of phosphorus tribromide in 700 ml of n-pentane and the mixture is stirred at room temperature for 3 hours. The mixture is poured on to 500 g of ice and stirred up for 30 minutes. The pentane phase is separated and the aqueous phase is back-extracted with n-pentane. The combined n-pentane phases are washed neutral with saturated sodium bicarbonate solution and water, dried over sodium sulphate and evaporated. The 3-(p-tert.butyl-phenyl)-2-methyl-allyl bromide, distilled in a high vacuum, boils at 123° C./0.01 Torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04241058 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-c790d7e2e6e84c52b4a53e8f8046ec12 |
| Source note | uspto-grants-1980_12 |