HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzylpiperidine → 4-Benzyl-1-(2-(4-benzyloxy-3-nitrophenoxy)ethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzylpiperidine | HCID 31738 | — |
| Reactant | 2-(4-Benzyloxy-3-nitrophenoxy)ethyl bromide | HCID 23294404 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Benzyl-1-(2-(4-benzyloxy-3-nitrophenoxy)ethyl)piperidine | HCID 23294452 | 77.1% |
Reaction Steps
From a mixture of 4-benzylpiperidine (2.68 9, 15.1 mmol), 2-(4-benzyloxy-3-nitrophenoxy)ethyl bromide (2.65 g, 7.52 mmol) and KI (110 mg) in toluene (25 mL) was obtained 2.59 g (77%) of 4-benzyl-1-(2-(4-benzyloxy-3-nitrophenoxy)ethyl)piperidine as an orange-yellow oil. 1H NMR (CDCl3): 1.30-1.42 (m, 2H), 1.50-1.60 (m, 1H), 1.64-1.68 (m, 2H), 2.02-2.10 (m, 2H), 2.547 (d, 2H, J=7), 2.777 (t, 2H, T=6), 2.95-3.00 (m, 2H), 4.085 (t, 2H, J=6), 5.181 (s, 2H), 7.02-7.46 (m, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124323 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-015a2e03db4545e89522ea4ccdaea661 |
| Source note | uspto-grants-2000_09 |