HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 3-(Bromomethyl)-1-ethylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | (1-Ethylpiperidin-3-yl)methanol | HCID 20439432 | — |
| Product | 3-(Bromomethyl)-1-ethylpiperidine | HCID 21510488 | — |
Reaction Steps
A mixture of 5.0 g. (0.0349 mol.) of N-ethyl-3-hydroxymethylpiperidine and 52 ml. of 48% hydrogen bromide was refluxed for six hours then cooled and evaporated to dryness. The residue was made basic by addition of 5% aqueous sodium carbonate and extracted with methylene chloride. The methylene chloride solution was dried (MgSO4) and evaporated to dryness to give 3-bromomethyl-N-ethylpiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983245 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-fd0be05369d74970bcb79e0ff8cda00c |
| Source note | uspto-grants-1976_09 |