HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Butyric acid, 4-piperidino-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-(piperidin-1-yl)butanoate | HCID 14044356 | — |
| Solvent | Water | HCID 962 | — |
| Product | Butyric acid, 4-piperidino- | HCID 20794 | — |
Reaction Steps
To a suspension of crude 4-piperidin-1-yl-butyric acid ethyl ester from the previous step (about 25 mmol) in 15 mL of water, NaOH (1.4 g, 25 mmol) was added and the mixture was heated at reflux for 16 hours. The reaction was then allowed to cool down to room temperature, the solution was acidified at 0° C. with HCl 6N and concentrated under reduced pressure. The residue was treated with EtOH and the sodium chloride which precipitated was filtered off. Evaporation of the solvent under reduced pressure afforded 2.8 g of the title compound as a white solid in 58% overall yield of steps a) and b)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163729B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-ca918bfda42744248bc7a6e0ffabd6bf |
| Source note | uspto-grants-2012_04 |