HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 10740172, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 11373410 | HCID 11373410 | — |
| Product | HCID 10740172 | HCID 10740172 | 66.5% |
Reaction Steps
Working again according to a protocol identical to the one used in step 1.1 of Example 1, followed by treating, under the same conditions as those of step 1.2 of Example 1, 1 g of 1,4-dibenzyl-2-phenoxycarbonyloxymethylpiperazine with 10 ml de piperidine, 0.68 g of 1,4-dibenzyl-2-(1′-piperidinocarbonyloxymethyl)piperazine is obtained in the form of a viscous product. Yield: 66.5%. Rf=0.09 (70/30 v/v ether/petroleum ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06531476B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-f9908d8baf66463fbed1c9e603b5312b |
| Source note | uspto-grants-2003_03 |