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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-Bromo-2-(methylsulfanyl)pyrimidineHCID 4738564—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-Bromo-2-(methylsulphonyl)pyrimidineHCID 31928680%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642611B2
Source datasetuspto-grants-2014_02
ORD IDord-77fbdd72c5e5446085374e1d3c8899cc
Source noteuspto-grants-2014_02