HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-Benzylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Benzylpiperidine | HCID 76190 | — |
Reaction Steps
A mixture of 11.9 ml of benzyl bromide in 100 ml of ether was added dropwise to a solution of 29.6 ml of piperidine in 100 ml of ether. This mixture was stirred overnight, then filtered. The organic layer was washed with water, then dried and concentrated to an oil. The oil was distilled through a Kugelrohr and the fraction boiling at 75°-85° C., 1.55 mm collected, giving 16.77 g of 1-(phenylmethyl)piperidine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892885 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-99b2b5e6ae394abdbcb70a51eda9a09e |
| Source note | uspto-grants-1990_01 |