HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714146Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 58149524, compound
https://huagongshe.com/reaction/714146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | 2,2-Dimethyl-1-(pyrimidin-5-yl)propan-1-one | HCID 13645650 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58149524 | HCID 58149524 | — |
Reaction Steps
Under an atmosphere of argon, 10 ml of dimethyl sulphoxide are slowly added dropwise to 0.96 g (4.3 mmol) of trimethylsulphoxonium iodide and 0.17 g of sodium hydride (60%, 4.3 mmol). The reaction mixture is then stirred at room temperature for 15 min, and 0.65 g (3.9 mmol) of 2,2-dimethyl-1-(5-pyrimidinyl)-1-propanone, dissolved in 2 ml of tetrahydrofuran, is added. The reaction mixture is stirred at 50° C. for 90 min. The reaction mixture is then concentrated under reduced pressure, and saturated aqueous sodium chloride solution and ethyl acetate are added to the residue. The organic phase is separated off, dried with sodium sulphate, filtered and concentrated. This gives 0.70 g (99%) of the desired product, which is reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187431B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-781c71d9a53842b5a2eb37ac33e4a01f |
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| Source note | uspto-grants-2015_11 |
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