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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587118Generated: October 27, 2026

Sodium Bicarbonate → Tert-butyl 2-hydroxy-7-azaspiro[3.5]nonane-7-carboxylate

https://huagongshe.com/reaction/587118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantTert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylateHCID 11195798—
SolventMethanolHCID 887—
ProductTert-butyl 2-hydroxy-7-azaspiro[3.5]nonane-7-carboxylateHCID 983467757%

Reaction Steps

To a solution of tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate (600 mg, 2.5 mmol, 1.0 equiv) in MeOH (6.0 mL) was added sodium borohydride (190 mg, 5.0 mmol, 2.0 equiv) in portions at 0° C. under nitrogen. The mixture was stirred at room temperature for 2.0 hrs. The solution was concentrated by evaporator to give the white solid. Saturated NaHCO3 solution (40 mL) was added. The aqueous phase was extracted with DCM (4×30 mL). The combined organic phase was dried over anhydrous Na2SO4, concentrated to give the crude which was purified by CombiFlash (24 g silica gel column, EtOAc/Hexane=0-60%) to afford 334 mg (yield 57%) of tert-butyl 2-hydroxy-7-azaspiro[3.5]nonane-7-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226923B2
Source datasetuspto-grants-2016_01
ORD IDord-f8c888775fca44afa279ba566c711b7b
Source noteuspto-grants-2016_01