HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Benzene, 1-bromo-4-(3-bromo-2-methyl-1-propen-1-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 54151335 | HCID 54151335 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzene, 1-bromo-4-(3-bromo-2-methyl-1-propen-1-yl)- | HCID 68710435 | 98% |
Reaction Steps
To an acetonitrile solution (180 mL) of triphenylphosphine (24.3 g, 92.7 mmol) was added dropwise bromine (4.78 mL, 185 mmol) at 0° C. and the mixture was stirred at the same temperature for 30 minutes. To the solution was added the acetonitrile solution (60 mL) of 3-(4-bromophenyl)-2-methyl-2-propen-1-ol obtained in Reference Example 106 (20.1 g, 88.3 mmol) and the mixture was stirred at 0° C. for 1 hour. The reaction solution was concentrated under reduced pressure, diethyl ether (200 mL) was added to the residue, and the insolubles were filtered off. The solution was washed with a saturated brine, dried over sodium sulfate, and then concentrated under reduced pressure to obtain 25.0 g (yield 98%) of the title compound as an oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07465815B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-17daa7386f1c4f418cebac2e1186f3e3 |
| Source note | uspto-grants-2008_12 |