HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 1-(1-Methyl-3-bromopropyl)piperidine hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1-(1-Methyl-3-phenoxypropyl)piperidine | HCID 20135812 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(1-Methyl-3-bromopropyl)piperidine hydrobromide | HCID 20135903 | 75% |
Reaction Steps
5 g of the 1-(1-methyl-3-phenoxypropyl)piperidine thus obtained was reacted with 30 ml of 40% hydrobromic acid at 150° C for 7 hours with stirring. The reaction solution was cooled and added with 20 ml of chloroform. Then, the hydrobromic acid layer was separated from the chloroform layer. The hydrobromic acid was removed under reduced pressure and the residue was recrystallized from 5 ml of ethyl alcohol to give 4.84 g of 1-(1-methyl-3-bromopropyl)piperidine hydrobromide in a yield of 75%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04751302 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-282115b3b02a4995813bd1bcfe2029c4 |
| Source note | uspto-grants-1988_06 |