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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7645Generated: October 25, 2026

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

https://huagongshe.com/reaction/7645

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, 14, (19 9,86.1 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 numberUS07087615B2
Source datasetuspto-grants-2006_08
ORD IDord-dead07a44f7a4bb99af3704ce3bf4d5d
Source noteuspto-grants-2006_08