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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588702Generated: October 29, 2026

Sulfoxonium, trimethyl-, iodide (1:1) → Benzyl 8-azaspiro[bicyclo[3.2.1]octane-3,2'-oxirane]-8-carboxylate

https://huagongshe.com/reaction/588702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant3-Oxo-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid benzyl esterHCID 14682535—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 8-azaspiro[bicyclo[3.2.1]octane-3,2'-oxirane]-8-carboxylateHCID 74394144—

Reaction Steps

To a 500-mL, three-necked, round-bottomed flask equipped with a magnetic stirring bar, a thermometer, and a condenser was charged tetrahydrofuran (163 mL), potassium tert-butoxide (6.6 g, 95% pure) and trimethylsulfoxonium iodide (13.0 g). The mixture was heated to reflux and stirred for 3 hours. A solution of benzyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate (10.0 g) in tetrahydrofuran (37 mL) was added in one portion. The reaction mixture was refluxed for another 2 hours. The mixture was cooled to room temperature and diluted with toluene (100 mL) and water. The water layer was separated and extracted with toluene (2×50 mL). The combined organic layers were washed with water (3×40 mL) and concentrated under vacuum to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227963B2
Source datasetuspto-grants-2016_01
ORD IDord-c157054e46074500a0f7243282a06da7
Source noteuspto-grants-2016_01