Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253721Generated: October 30, 2026

Sodium borohydride → Tert-butyl 9-(2-hydroxyethoxy)-3-azaspiro[5.5]undecane-3-carboxylate

https://huagongshe.com/reaction/1253721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 9-(2-oxoethoxy)-3-azaspiro[5.5]undecane-3-carboxylateHCID 86645836—
SolventMethanolHCID 887—
ProductTert-butyl 9-(2-hydroxyethoxy)-3-azaspiro[5.5]undecane-3-carboxylateHCID 6670097640%

Reaction Conditions

Temperature25 °C

Reaction Steps

NaBH4 (13.46 mmol, 2.0 eq.) was added portion wise to a stirred solution of tert-butyl 9-(2-oxoethoxy)-3-azaspiro[5.5]undecane-3-carboxylate (6.73 mmol, 1.0 eq.) in MeOH (65 ml) at 0° C. and the resulting reaction mixture was stirred at 25° C. for 16 h. The solvent was evaporated under reduced pressure. The residue was dissolved in ethyl acetate (300 ml) and washed with water (200 ml) and brine (200 ml). The organic layer was dried over sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography eluting with 20% ethyl acetate in hexanes to give the desired product as a yellow sticky solid. Yield: 40%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455475B2
Source datasetuspto-grants-2013_06
ORD IDord-c0815286f4cd4c0baf17e42dd44103ce
Source noteuspto-grants-2013_06