HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → Benzyl 4-(bromomethyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 736490 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 4-(bromomethyl)piperidine-1-carboxylate | HCID 2776274 | 89.9% |
Reaction Steps
To a solution of 4-hydroxymethylpiperidine-1-carboxylic acid benzyl ester (1.11 g), carbon tetrabromide (1.77 g) in methylene chloride (11 ml) was added triphenylphosphine (1.4 g) with ice-cooling, and the mixture was stirred at room temperature for 5 hours. After completion of the reaction, the solvent was evaporated and the obtained residue was purified by silica gel column chromatography (hexane:acetone=10:1) and dried under reduced pressure to give the title compound (1.25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562828B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-712740cb1d5a420db17ae984c0c3ade2 |
| Source note | uspto-grants-2003_05 |