HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-(5-Bromo-3-methyl-2-pyridinyl)butylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfur trioxide | HCID 24682 | — |
| Reactant | HCID 23325013 | HCID 23325013 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Cfc 113 | HCID 6428 | — |
| Product | 4-(5-Bromo-3-methyl-2-pyridinyl)butylamine | HCID 13094272 | 51.5% |
Reaction Steps
A solution of sulphur trioxide (150 ml) in 1,1,2-trifluorotrichloroethane (350 ml) was added over ca 30 min. to a suspension of 4-(3-methyl-2-pyridyl)butylamine dihydrobromide (17 g) [prepared by passing hydrogen bromide gas through a solution of the amine in dichloromethane] in 1,1,2-trifluorotrichloroethane (100 ml) and the mixture was heated under reflux for ca 16 hr. The solvent was removed by distillation and unbrominated starting material was removed by acetylation as described in Example 1(b) to yield 4-(5-bromo-3-methyl-2-pyridyl)-butylamine (6.53 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515952 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-145153409f4d4cddaf72f583e286a52d |
| Source note | uspto-grants-1985_05 |