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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981296Generated: October 31, 2026

Ethanol → Ethyl trans-4-azido-3-hydroxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/981296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium AzideHCID 33557—
ReactantEthyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylateHCID 12414163—
SolventWaterHCID 962—
ProductEthyl trans-4-azido-3-hydroxy-1-piperidinecarboxylateHCID 1367784680%
ProductEthyl trans-3-azido-4-hydroxy-1-piperidinecarboxylateHCID 8674457515%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990521
Source datasetuspto-grants-1991_02
ORD IDord-3b854a9f83a546ed92745f920b3d07bf
Source noteuspto-grants-1991_02