HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Chloro-5-(methylsulphonyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Chloro-5-(methylsulfanyl)benzoic acid | HCID 608814 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Product | 2-Chloro-5-(methylsulphonyl)benzoic acid | HCID 2329132 | — |
Reaction Steps
To 99 mmol 2-chloro-5-(methylthio) benzoic acid in 400 ml methanol at 0° C. 296 mmol oxone® was added, and the mixture was allowed to stir at RT for 3.5 h. The precipitate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was extracted 3 x with 400 ml ethyl acetate, and the combined organic phases washed 2× with 300 ml 1N HCl and with 300 ml saturated aqueous NaCl solution and dried with MgSO4. Evaporation under reduced pressure yielded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429585B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-820c8857e46f46e6a1beb45e001726a8 |
| Source note | uspto-grants-2008_09 |