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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430284Generated: November 1, 2026

Cycloheptanone → 1-oxaspiro[2.6]nonane

https://huagongshe.com/reaction/1430284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCycloheptanoneHCID 10400—
ReactantTrimethylsulfonium iodideHCID 75127—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product1-oxaspiro[2.6]nonaneHCID 642941—

Reaction Steps

To a mixture of trimethylsulfonium iodide (35.7 g) in 300 mL dry DMSO was added 11.2 g of cycloheptanone with stirring. A solution of potassium tert-butoxide (16.83 g) in 200 mL dry DMSO was slowly added. The resulting solution was stirred at room temperature for 16 hours. The reaction mixture was quenched by addition of water (600 mL), and extracted with diethyl ether (3×200 mL). The combined organic layers were washed with water (200 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940737B2
Source datasetuspto-grants-2015_01
ORD IDord-013fb8225341426c88f999078c014c2b
Source noteuspto-grants-2015_01