HuagongsheHuagongshe Chemistry Print Report · For research reference only
MeOH tetrahydrofuran → Methyl 2-(methylsulfonyl)pyrimidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 2-Methyl-sulfanyl-pyrimidine-4-carboxylic acid methyl ester | HCID 69222019 | — |
| Product | Methyl 2-(methylsulfonyl)pyrimidine-4-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087615B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-dead07a44f7a4bb99af3704ce3bf4d5d |
| Source note | uspto-grants-2006_08 |