Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461341Generated: October 31, 2026

Methyl iodide → HCID 19980408, compound

https://huagongshe.com/reaction/1461341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10398927HCID 10398927—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19980408HCID 1998040890.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

8-Ethoxycarbonyl-3-hydroxy-1-oxa-8-azaspiro[4.5]decane (1 g, 0.0044 mol) was dissolved in anhydrous THF (40 ml) under nitrogen and cooled with an ice-bath. Sodium hydride (0.22 g, 5.5 mmol as a 60% oil dispersion) was added and the reaction was stirred at 0° C. for 20 minutes. Methyl iodide (2.0 g, 0.9 ml) in THF (10 ml) was added dropwise. The reaction was allowed to warm to room temperature and stirred for 3 hours. An additional 0.9 ml of methyl iodide was added at 0° C. and stirring was continued overnight. The cooled reaction was diluted with water (10 ml). The aqueous THF was washed with saturated brine and dried over Na2SO4. The solvents were evaporated and the residue was purified by flash chromatography on silica gel by elution with ammoniated 2% methanol/chloroform. Evaporation of the solvents gave 0.97 g of a pale orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075317
Source datasetuspto-grants-1991_12
ORD IDord-d76fee9250bb452eaf58e71fc2bab23f
Source noteuspto-grants-1991_12