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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413035Generated: October 25, 2026

MeOH tetrahydrofuran → Methyl 2-(methylsulfonyl)pyrimidine-4-carboxylate

https://huagongshe.com/reaction/413035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMeOH tetrahydrofuranHCID 21899815—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant2-Methyl-sulfanyl-pyrimidine-4-carboxylic acid methyl esterHCID 69222019—
ProductMethyl 2-(methylsulfonyl)pyrimidine-4-carboxylateHCID 19868790—

Reaction Steps

An aqueous solution (1 L) of Oxone® (211.7 g, 344 mmol) is added dropwise at 0° C. to a solution of 2-methyl-sulfanyl-pyrimidine-4-carboxylic acid methyl ester, 12, (19 g,86.1 mmol) in 1:1 methanol/THF (1 L). The reaction solution is allowed to warm to room temperature and stir for 1.5 hours. The resulting suspension is partitioned between methylene chloride and water. The aqueous phase is made alkaline with the addition of NaOH and re extracted with solvent. The combined organic layers are dried, filtered, and concentrated in vacuo to afford 18.4 g of the desired product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566357B1
Source datasetuspto-grants-2003_05
ORD IDord-ee19468f27494275b23a4a2ad93219ad
Source noteuspto-grants-2003_05