HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 18919865, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | alpha-Bromo-o-chlorotoluene | HCID 11905 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18919865 | HCID 18919865 | 62% |
Reaction Steps
0.202 g (0.002 mol) of 4-hydroxypiperidine, 1.22 ml (0.0088 mol) of triethylamine and 0.43 g (0.0021 mol) of 2-chlorobenzyl bromide were dissolved in 5 ml of dimethylform-amide and stirred at room temperature for 2 hrs. The solvent was distilled off and the residue was taken up in dichloromethane and washed with saturated bicarbonate solution and sodium chloride solution. The organic phase was dried over sodium sulfate and concentrated. 0.28 g (62%) 1-(2-chloro-benzyl)-piperidin-4-ol was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753679 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-a54a0efb460545a9b63bef9bf0de3f8b |
| Source note | uspto-grants-1998_05 |