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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943596Generated: November 2, 2026

Sodium borohydride → tert-Butyl 6-hydroxy-2-azaspiro[3.3]heptane-2-carboxylate

https://huagongshe.com/reaction/1943596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 6-oxo-2-azaspiro(3.3)heptane-2-carboxylateHCID 52333005—
SolventMethanolHCID 887—
Producttert-Butyl 6-hydroxy-2-azaspiro[3.3]heptane-2-carboxylateHCID 5298776596.4%

Reaction Steps

0.494 g (13.06 mmoles) of sodium borohydride is added in portions at 0° C. to a solution of 2.30 g (10.89 mmoles) of tert-butyl 6-oxo-2-aza-spiro[3.3]-heptane-2-carboxylate, obtained in stage 10.2, in 55 ml of methanol. The reaction mixture is stirred for 1 hr 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 dichloromethane, and the combined organic phases are washed with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and the filtrate is concentrated under reduced pressure. After crystallisation of the residue in diisopropyl ether, filtration of the solid obtained and drying under vacuum at 60° C., 2.24 g of product are obtained in the form of a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394787B2
Source datasetuspto-grants-2013_03
ORD IDord-948839cdea534bba9b3369148721ace5
Source noteuspto-grants-2013_03