HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378931Generated: November 3, 2026
1-Benzyl-4-piperidylamine → N-(2-nitrophenethyl)-1-benzylpiperidin-4-amine
https://huagongshe.com/reaction/2378931
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | 2-Nitrophenethyl bromide | HCID 12363878 | — |
| Product | N-(2-nitrophenethyl)-1-benzylpiperidin-4-amine | HCID 16202487 | 81% |
Reaction Steps
1-(2-Bromoethyl)-2-nitrobenzene (1.5 g, 6.52 mmol) and 4-amino-1-benzylpiperidine (3.0 ml, 14.71 mmol) were combined. Mixture was heated neat at 100° C. and held with stirring for 17 hours. Mixture was cooled to room temperature. Residue was triturated in 30 mL diethyl ether. Solids were filtered off, washed with diethyl ether and discarded. Filtrate was concentrated. Silica gel chromatography on the residue eluting 2M ammonia in methanol-dichloromethane afforded the title compound as brown oil in 81% yield. MS (M+H)+=340.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07470680B2 |
|---|
| Source dataset | uspto-grants-2008_12 |
|---|
| ORD ID | ord-2bb46510d6104a88951902a499dc8a15 |
|---|
| Source note | uspto-grants-2008_12 |
|---|