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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943593Generated: November 1, 2026

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

https://huagongshe.com/reaction/1943593

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 mmoles) of sodium borohydride is added in portions at 0° C. to a solution of 3.54 g (15.71 mmoles) of tert-butyl 2-oxo-6-aza-spiro[3.4]octane-6-carboxylate (WO 9806720) diluted in 40 ml of methanol. The reaction mixture is stirred for 1 hr and 30 mins at ambient temperature. After evaporation of the solvent, water is added to the reaction mixture, the aqueous phase is separated, it is extracted several times with diethyl ether, and the combined organic phases are washed with a saturated aqueous solution of sodium chloride, they are dried over sodium sulphate and the filtrate is concentrated under reduced pressure. After evaporation of the solvent, 3.10 g of product are obtained in the form of a brown oil used as such in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394787B2
Source datasetuspto-grants-2013_03
ORD IDord-88576e71fd4442368b89b695746eca49
Source noteuspto-grants-2013_03