HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1-Benzyl-4-(dimethylamino)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Benzyl-4-(dimethylamino)piperidine | HCID 416066 | 80% |
Reaction Steps
To a solution of 4-amino-1-benzylpiperidine (1.47 g, 7.7 mmol) in CF3 CH2OH (14 ml) were added molecular sieve 4 Å (5), and paraformaldehyde (0.51 g, 17 mmol). After stirring at RT for 1 h, NaCNBH3 (2.5 g, 39.8 mmol) was added and stirred for 16 h at RT. The reaction was stopped by addition of H2O and the product was extracted with (4:1) (Et2O:CH2Cl2). Organic fractions were combined and washed with brine (2×), dried over MgSO4, filtered and concentrated to give a crude material which was purified by silica flash chromatography to afford 4-dimethylamino-1-benzylpiperidine (80% yield). FAB Mass [M+1]+35Cl 219.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05795894 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-791b78be97ce41668cf52ff92dd661ff |
| Source note | uspto-grants-1998_08 |