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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | 4-(Propan-2-ylidene)cyclohexan-1-one | HCID 12691196 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 86704997 | HCID 86704997 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09211269B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-ed9b314357764b858370315c32ac74b4 |
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| Source note | uspto-grants-2015_12 |
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