HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | tert-Butyl 4-(3-ethoxy-3-oxopropyl)piperidine-1-carboxylate | HCID 23245138 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)propanoic acid | HCID 1512540 | — |
Reaction Steps
A solution of KOH (86%, 0.42 g, 6.4 mmol) in water (1.5 mL) was added to a solution of 3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propionic acid ethyl ester in 95% EtOH (15 mL) at rt. After 2.5 h, the mixture was partitioned between EtOAc (50 mL) and 2 N aq. HCl (50 mL). After extraction of the aqueous layer with EtOAc (50 mL), the organic layers were washed with sat'd NaCl (25 mL), dried (Na2SO4), decanted, and evaporated to give 1.06 g of the title compound as a crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399619B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-84ac710993d7447f9f634083b8ed4d4f |
| Source note | uspto-grants-2002_06 |