HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-(tert-Butoxycarbonyl)-4-(trifluoromethyl)piperidine-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21054722 | HCID 21054722 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(tert-Butoxycarbonyl)-4-(trifluoromethyl)piperidine-4-carboxylic acid | HCID 17983139 | — |
Reaction Steps
A solution of ethyl 1-(tert-butoxycarbonyl)-4-(trifluoromethyl)piperidine-4-carboxylate (3b) (1 equiv.) and 1.0 N NaOH (1.2 equiv.) in EtOH is heated at 50° C. When the reaction is complete, the solvents are removed in vacuo, and the residue is taken up in H2O. The solution is acidified to pH 5-6 with dilute HCl, and the precipitate is collected and washed with H2O. Drying in high vacuum gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312212B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-780cad8114be4ebfbba7c194e69bc2da |
| Source note | uspto-grants-2007_12 |