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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336524Generated: October 30, 2026

Sodium borohydride → tert-Butyl 2-hydroxy-6-azaspiro(3.4)octane-6-carboxylate

https://huagongshe.com/reaction/336524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 2-oxo-6-azaspiro[3.4]octane-6-carboxylateHCID 23565399—
SolventMethanolHCID 887—
Producttert-Butyl 2-hydroxy-6-azaspiro(3.4)octane-6-carboxylateHCID 69669842—

Reaction Steps

0.89 g (23.57 mmol) of sodium borohydride is added portionwise at 0° C. to a solution of 3.54 g (15.71 mmol) of tert-butyl 2-oxo-6-azaspiro[3.4]octane-6-carboxylate (WO98/06720) diluted in 40 mL of methanol. The reaction mixture is stirred at room temperature for 1 hour 30 minutes. After evaporating off the solvent, water is added to the reaction medium, the aqueous phase is separated out and extracted several times with diethyl ether, the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the filtrate is concentrated under reduced pressure. After evaporating off the solvent, 3.10 g of product are obtained in the form of a brown oil, which is used without further purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889702B2
Source datasetuspto-grants-2014_11
ORD IDord-7b09093e6ff742c69ee3aaf29fd5631f
Source noteuspto-grants-2014_11