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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383540Generated: October 30, 2026

Dimethyl Sulfoxide → 1,1-Dimethyl-4-methylidenecyclohexane

https://huagongshe.com/reaction/383540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
ReactantCyclohexanone, 4,4-dimethyl-HCID 138166—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
Product1,1-Dimethyl-4-methylidenecyclohexaneHCID 572964—

Reaction Steps

Methyltriphenylphosphonium bromide (2.97 g, 8.3 mmol) was added in the dehydrated DMSO (8 mL) solution of sodium hydride (0.35 g, 8.7 mmol) in an ice bath. The reaction mixture was stirred at room temperature for 10 minutes, and the dehydrated DMSO solution (1.5 mL) of 4,4-dimethyl-cyclohexanone (1.0 g, 7.9 mmol) was added slowly in an ice bath. The reaction mixture was stirred at room temperature for 18 hours and poured into ice water. The organic layer was extracted with diethyl ether, and then the layer was washed with water and dried with anhydrous magnesium sulfate, and removed by filtration. The filtrate was concentrated until becoming about half in volume. The formed insoluble matter was removed by filtration, then the filtrate was removed by distillation under reduced pressure, and colorless oily matter (0.91 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367666B2
Source datasetuspto-grants-2013_02
ORD IDord-b240ccb3ab5c4d388bb6e2ad0a60ee86
Source noteuspto-grants-2013_02