HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Piperidinecarboxylic acid → 1-(Ethoxycarbonyl)-4-piperidinecarboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Piperidinecarboxylic acid | HCID 3773 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(Ethoxycarbonyl)-4-piperidinecarboxylic Acid | HCID 6618886 | — |
Reaction Steps
4-Carboxy-1-ethoxycarbonylpiperidine is prepared from piperidine-4-carboxylic acid (Aldrich, Steinheim, FRG), for example by reacting piperidine-4-carboxylic acid with ethyl chloroformate in aqueous sodium hydroxide solution for 2 h at from 0° to 5° C. The title compound is extracted from the aqueous phase by shaking with toluene. The toluene phase containing the dissolved title compound is dried over Na2SO4 and directly subjected to further use.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05807891 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-e8dee184d311480bbb3c5c961f7c094e |
| Source note | uspto-grants-1998_09 |