HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Benzyl-piperidin-4-yl 4-nitro-benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 1-Benzylpiperidin-4-ol | HCID 78461 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Benzyl-piperidin-4-yl 4-nitro-benzoate | HCID 18919816 | 106.1% |
Reaction Steps
0.5 g (0.00216 mol) of 1-benzyl-4-hydroxypiperidine and 0.64 ml (0.0046 mol) of triethylamine were dissolved in 20 ml of toluene, treated with 0.5 g (0.0027 mol) of 4-nitro-benzoyl chloride and boiled at reflux for 6 hrs. The suspension was filtered, the filtrate was concentrated and the residue was chromatographed over silica gel with ethyl acetatelhexane (1:3) as the eluent. 0.78 g (85%) of 1-benzyl-piperidin-4-yl 4-nitro-benzoate was obtained as yellow crystals; m.p. 87°-89°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753679 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-2eb1e9d417994a7ebcba4774e1006ae2 |
| Source note | uspto-grants-1998_05 |