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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494160Generated: October 30, 2026

Sodium hydride → HCID 59657472, compound

https://huagongshe.com/reaction/494160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantCyclohexane, (bromomethyl)-HCID 137636—
ReactantHCID 13016609HCID 13016609—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59657472HCID 5965747265%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 5.0 g 4-butyl-2-oxo-1-oxa-3,8-diaza-spiro[4.5]decane-8-carboxylic acid benzyl ester (14.4 mmol) in 50 mL DMF was added 994 mg of sodium hydride (21.6 mmol, 60% dispersion in mineral oil). The reaction mixture stirred for five minutes and 2.2 mL of cyclohexylmethyl bromide (15.8 mmol) was then added. The reaction mixture stirred under nitrogen for 18 h. The reaction mixture was heated to 70° C. for three h. The reaction mixture cooled to room temperature and was diluted with 500 mL EtOAc and washed twice with water, once with brine. The organics were dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel utilizing a gradient elution (10% to 15% EtOAc/DCM) to provide 4.1 g (65%) of 4-butyl-3-cyclohexylmethyl-2-oxo-1-oxa-3,8-diaza-spiro[4.5]decane-8-carboxylic acid benzyl ester: ms [M]+=443.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538122B2
Source datasetuspto-grants-2009_05
ORD IDord-bda7f4f6bd7a4ed1a8361b0514c2fc9d
Source noteuspto-grants-2009_05