HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372658Generated: November 3, 2026
Dimethyl Sulfoxide → HCID 178493554, compound
https://huagongshe.com/reaction/2372658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | 4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine | HCID 838363 | — |
| Reactant | HCID 19823894 | HCID 19823894 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178493554 | HCID 178493554 | — |
Reaction Steps
0.55 g (4.9 mmol) of potassium tert-butylate is added a little at a time to a solution of 0.6 g (2.4 mmol) of 6-phenylthiosalicylic acid in 8 ml of dimethyl sulfoxide, the temperature increasing to 35° C. The mixture is cooled to room temperature, after which 0.53 g (2.4 mmol) of 4,6-dimethoxy-2-methylsulfonylpyrimidine is added and stirring is carried out for one hour at room temperature. The content of the flask is poured onto a mixture of 100 ml of cold water, 1 ml of orthophosphoric acid and 50 ml of ether. The ether phase is washed with 5% strength phosphoric acid and water, dried and evaporated down. After the crude product has been stirred with cold toluene, 0.50 g (54%) of the above product of melting point 135°-136° C. is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05100458 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-7298047da7d2498b95b81b12fd3db452 |
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| Source note | uspto-grants-1992_03 |
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