Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
MeOH tetrahydrofuran → Methyl 2-(methylsulfonyl)pyrimidine-4-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | MeOH tetrahydrofuran | HCID 21899815 | — |
| 반응물 | Potassium hydroxy sulfite | HCID 23707502 | — |
| 반응물 | 2-Methyl-sulfanyl-pyrimidine-4-carboxylic acid methyl ester | HCID 69222019 | — |
| 생성물 | Methyl 2-(methylsulfonyl)pyrimidine-4-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07087615B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-dead07a44f7a4bb99af3704ce3bf4d5d |
| 출처 메모 | uspto-grants-2006_08 |