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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494162Generated: October 29, 2026

Acetic Acid → HCID 25057601, compound

https://huagongshe.com/reaction/494162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmoniaHCID 222—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 20427870HCID 20427870—
ReactantHCID 59657483HCID 59657483—
SolventDichloromethaneHCID 6344—
ProductHCID 25057601HCID 2505760173%

Reaction Steps

To a solution of 4-butyl-1-oxa-3,8-diaza-spiro[4.5]decane-2-one (12: R=H; R′=n-Bu; 1.09 g; 5.1 mmol)) in 30 mL DCM was added 1.24 g (5.4 mmol) of 1-(2,6-dimethyl-benzoyl)-piperidin-4-one followed by 2.1 mL (7.1 mmol) of Ti(IV)(O-i-Pr)4 The reaction mixture stirred under nitrogen for 18 h. of Sodium triacetoxyborohydride (1.6 g: 7.7 mmol) was added to the reaction mixture followed by glacial HOAc (0.365 mL; 6.4 mmol). The reaction mixture stirred for 24 h. Aqueous ammonia (20 mL; 10% aqueous solution) was added and the solution stirred for an additional 10 min. The mixture was filtered by gravity through a cartridge of ChemElute™. The organics were evaporated under reduced pressure and the residue was purified by flash chromatography on silica gel with gradient elution (2% to 10% methanol in ethyl acetate with 0.4% ammonia) to provide 1.6 g (73%) of 4-butyl-8-[1-(2,6-dimethyl-benzoyl)-piperidin-4-yl]-1-oxa-3,8-diaza-spiro[4.5]decane-2-one: ms [M]+=428.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538122B2
Source datasetuspto-grants-2009_05
ORD IDord-30fbf80bd12741bca97030604c9c65bf
Source noteuspto-grants-2009_05