HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238151Generated: October 29, 2026
Sodium Hydroxide → 5-Bromo-2-(methylsulphonyl)pyrimidine
https://huagongshe.com/reaction/238151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Bromo-2-(methylsulfanyl)pyrimidine | HCID 4738564 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-2-(methylsulphonyl)pyrimidine | HCID 319286 | 80% |
Reaction Steps
To a solution of 5-bromo-2-methylsulfanylpyrimidine (10.0 g, 48.8 mmol) in methanol (195 mL) were added a solution of Oxone® (94.6 g, 154 mmol, 3.16 eq) in water (500 mL and aq. 4 N sodium hydroxide (40 mL, 160 mmol, 3.28 eq.) portionwise and in an alternating addition mode to maintain pH between 2 and 3 at a temperature of 0° C. After complete addition, the mixture was allowed to stir for 2 h at room temperature. Water (500 mL) was added, and the mixture was extracted with ethyl acetate (2×500 mL). The aqueous layer was adjusted to pH 7 by addition of aq. sodium hydroxide, and was again extracted with ethyl acetate. The combined organic layers were dried over MgSO4 and evaporated to give 9.23 g (80% yield) of the desired sulfone which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642611B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-77fbdd72c5e5446085374e1d3c8899cc |
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| Source note | uspto-grants-2014_02 |
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