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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502620Generated: November 1, 2026

Sulfoxonium, trimethyl-, iodide (1:1) → HCID 86704997, compound

https://huagongshe.com/reaction/1502620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant4-(Propan-2-ylidene)cyclohexan-1-oneHCID 12691196—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86704997HCID 8670499777%

Reaction Steps

Potassium t-butoxide (3.3 g, 29.4 mmol) was added to a mixture of ketone (3, 2.5 g, 18.1 mmol) and trimethylsulfoxonium iodide (6.45 g, 29.4 mmol) in dry dimethyl sulfoxide (40 mL) under nitrogen atmosphere at room temperature. The mixture was stirred for 4.0 h at room temperature. The reaction was quenched by the addition of cold water (40 mL) and extracted with ethyl acetate (2×60 mL). The combined organic layer was washed with water (75 mL) followed by brine (75 mL) and dried over sodium sulfate. The filtered organic layer was concentrated under vacuum to give an oil. Weight: 2.13 g. Weight yield: 77%. 1H-NMR (400 MHz, CDCl3): δ 1.42-1.50 (m, 2H), 1.55-1.61 (m, 2H), 1.65 (s, 6H), 2.31 (t, 4H), 2.61 (s, 2H). MS (APCI method): No molecular ion peak was observed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211269B2
Source datasetuspto-grants-2015_12
ORD IDord-ed9b314357764b858370315c32ac74b4
Source noteuspto-grants-2015_12