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HRID 7645생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/7645

반응식

참여 물질

역할이름HCID투입량
반응물MeOH tetrahydrofuranHCID 21899815—
반응물Potassium hydroxy sulfiteHCID 23707502—
반응물2-Methyl-sulfanyl-pyrimidine-4-carboxylic acid methyl esterHCID 69222019—
생성물Methyl 2-(methylsulfonyl)pyrimidine-4-carboxylateHCID 19868790—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087615B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-dead07a44f7a4bb99af3704ce3bf4d5d
출처 메모uspto-grants-2006_08