HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobenzyl bromide → HCID 677772, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 677772 | HCID 677772 | 100% |
Reaction Steps
0.202 g (0.002 mol) of 4-hydroxypiperidine and 0.55 g (0.0022 mol) of 4-bromobenzyl bromide were dissolved in 5 ml of dimethylformamide and stirred at room temperature for 2 hrs. The solvent was distilled off and the residue was taken up in dichloromethane and washed with sat. bicarbonate solution and sodium chloride solution. The organic phase was dried over sodium sulfate and concentrated. 0.54 g (100%) of 1-(4-bromo-benzyl)-piperidin-4-ol was obtained as a colorless oil. MS: me/e (% basic peak)=271, 269 (C12H16BrNO30 , 73, 76), 270, 268 (79, 70), 171, 169 (99, 100), 114 (64), 100 (60).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753679 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-b0cce427147d4cf58f2bbf443e200515 |
| Source note | uspto-grants-1998_05 |