HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243991Generated: November 3, 2026
Sulfoxonium, trimethyl-, iodide (1:1) → HCID 21931845, compound
https://huagongshe.com/reaction/1243991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | 6-Methoxy-1-methyl-2(1H)-quinolinone | HCID 220459 | — |
| Reactant | HCID 178506865 | HCID 178506865 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 21931845 | HCID 21931845 | 107.8% |
Reaction Steps
A suspension of 3.35 gm (15.1 mmol) trimethylsulfoxonium iodide in 10 ml of THF at 0° C. under nitrogen was treated portionwise with 5.8 ml (14.6 mmol) of 2.5 M n-hexyllithium in heptane over 30 minutes. The mixture was stirred for 30 minutes at 0° C. and then treated with 1.0 gm (5.02 mmol) 6-Methoxy-1-methyl-1H-quinolin-2-one followed by heating under reflux for 1.5 hours. The reaction mixture was allowed to cool to ambient temperature before quenching with 35 ml of water followed by extraction into ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and evaporated to afford 1.1 gm of desired product. Mass spectrum APCI m/e 204 (p+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119207B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-64972da0117b461e92952d32eb6b5015 |
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| Source note | uspto-grants-2006_10 |
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