HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 16459886, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | N-(Phenylmethyl)-4-piperidinemethanamine | HCID 16004294 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 16459886 | HCID 16459886 | 50% |
Reaction Steps
Under ice-cooling, to 200 ml of a tetrahydrofuran (THF) solution containing 5.0 g of N-(4-piperidylmethyl)-N-benzylamine was added dropwise 50 ml of a THF solution containing 2.9 ml of benzyl bromide. After stirring the mixture at the same temperature for one hour, THF was removed from the reaction mixture under reduced pressure and a saturated sodium hydrogen carbonate aqueous solution was added to the residue. The mixture was extracted with ethyl acetate. The extract was washed and dried, and the solvent was removed under reduced pressure. Precipitated crystals were recrystallized from an ethanol solution to give 3.6 g of N-(1-benzylpiperidin-4-ylmethyl)-N-benzylamine (yield: 50%, melting point: 240° C. or higher).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849732 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-becb89b4c28341b3b0e97a7d16d6830a |
| Source note | uspto-grants-1998_12 |