HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl trans-4-azido-3-hydroxy-1-piperidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Ethyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate | HCID 12414163 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl trans-4-azido-3-hydroxy-1-piperidinecarboxylate | HCID 13677846 | 80% |
| Product | Ethyl trans-3-azido-4-hydroxy-1-piperidinecarboxylate | HCID 86744575 | 15% |
Reaction Steps
To a stirred emulsion of 53.8 parts of ethyl 7-oxa-3-azabicyclo-[4.1,0]heptane-3-carboxylate, 17.6 parts of ethanol and 195 parts of water were added portionwise, during a 15 minutes-period, 28.6 parts of sodium azide while cooling in an ice bath. The mixture was warmed slowly to room temperature and stirring was continued overnight at room temperature. The aqueous phase was separated and extracted twice with dichloromethane. The combined organic phases were washed with a small amount of water, dried, filtered and evaporated, yielding 56.3 parts (82%) of a mixture of 80% of ethyl trans- 4-azido-3-hydroxy-1-piperidinecarboxylate (interm. 3) and 15% of ethyl trans-3-azido-4-hydroxy-1-piperidinecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04990521 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-3b854a9f83a546ed92745f920b3d07bf |
| Source note | uspto-grants-1991_02 |