HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4-tert-butoxycarbonyl-1-(3,4,5-trimethoxybenzyl)piperazine-2-carboxylate → HCID 20066595, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4-tert-butoxycarbonyl-1-(3,4,5-trimethoxybenzyl)piperazine-2-carboxylate | HCID 20066667 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Product | HCID 20066595 | HCID 20066595 | — |
Reaction Steps
In 4.5N HCl-ethyl acetate solution (20 ml) is dissolved methyl 4-tert-butoxycarbonyl-1-(3,4,5-trimethoxybenzyl)piperazine-2-carboxylate (5.0 g) obtained in Reference Example 19, and the solution is left standing at room temperature for 5 hours. The reaction mixture is concentrated under reduced pressure to give crystalline methyl 1-(3,4,5-trimethoxybenzyl)-piperazine-2-carboxylate dihydrochloride (4.3 g). This product is recrystallized from ethanol to afford colorless needles, m.p. 170-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997836 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-55b4154227a7401bb2c71827223d4db7 |
| Source note | uspto-grants-1991_03 |