HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1-(3-Bromopropyl)-1,2,3,4-tetrahydronaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 57242163 | HCID 57242163 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Bromopropyl)-1,2,3,4-tetrahydronaphthalene | HCID 10399995 | 102% |
Reaction Steps
Compound 94-1 (140 mg) was dissolved in methylene chloride (10 ml), triphenylphosphine (212 mg) and N-bromosuccinimide (144 g) were added under ice-cooling, and the mixture was stirred under ice-cooling for 2 hr, and at room temperature 16 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 (50 ml) was added, and the precipitated triphenylphosphine oxide was filtered off. The concentrate of the filtrate was purified by silica gel column chromatography to give the object product (190 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129361B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-03abb45384e247e38a49a492c7603921 |
| Source note | uspto-grants-2012_03 |