HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-(3-Bromopropyl)-1,2-dimethoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(3',4'-Dimethoxyphenyl)-1-propanol | HCID 77528 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(3-Bromopropyl)-1,2-dimethoxybenzene | HCID 12765388 | 82.2% |
Reaction Steps
Compound 18-1 (2.00 g) was dissolved in methylene chloride (50 ml), triphenylphosphine (2.97 g) and N-bromosuccinimide (1.99 g) were added under ice-cooling, and the mixture was stirred under ice-cooling for 1 hr, and further at room temperature for 15 hr. The reaction mixture was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. Diethyl ether (100 ml) was added, and the precipitated triphenylphosphine oxide was filtered off. The concentrate of the filtrate was purified by silica gel column chromatography (hexane:ethyl acetate=5:1-3:1) to give the object product (2.17 g) as a pale-brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129361B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-009e9f1fbcaa4fd89150227d3b85821d |
| Source note | uspto-grants-2012_03 |