HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Piperic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Piperine | HCID 638024 | — |
| Solvent | Water | HCID 962 | — |
| Product | Piperic acid | HCID 5370536 | — |
Reaction Steps
To piperine (1) (2 g, 0.7 mmol, 1 eq), 20% of methanolic KOH (100 ml) was added and refluxed for 2 days. After completion of the hydrolysis, methanol was removed under reduced pressure and a yellow coloured oily solid was obtained. This residue was dissolved in water (50 ml) and acidified with 6N HCl to pH <1 yielding a yellowish precipitate of piperinic acid. Recrystallization from methanol gave yellow needles (0.9 g, 60% yield). m.p. 206°-208° C. (Lit m.p. 217 °-218° C.)1 2.2 Synthesis of Piperlonguminine (RV-A06)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122561B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-30e5bd05d6cd41b1ac869e20da2e1bb4 |
| Source note | uspto-grants-2006_10 |