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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259809Generated: October 31, 2026

Sulfoxonium, trimethyl-, iodide (1:1) → (5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)oxirane

https://huagongshe.com/reaction/2259809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant5,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-2-naphthalenecarbaldehydeHCID 10420887—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
Product(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)oxiraneHCID 14726539—

Reaction Steps

33 g (0.15 mole) of trimethylsulfoxonium iodide were added at room temperature to a solution of 17 g (0.15 mole) of potassium tert-butylate in 150 ml of dried dimethyl sulfoxide. The mixture was stirred for 0.5 hour, after which a solution of 32.5 g (0.15 mole) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthaldehyde in 100 ml of tetrahydrofuran was added dropwise. Stirring was continued for 1 hour, after which the mixture was poured onto water and extracted with ether. The organic phase was washed with water, dried over magnesium sulfate and evaporated down. 31.3 g of (5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-oxirane remained. The structure was determined by H-NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475017
Source datasetuspto-grants-1995_12
ORD IDord-cf6716d9c8494ea088f19699c329e65f
Source noteuspto-grants-1995_12