HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 1-Methyl-3-methylsulphinylmethyl-7-trifluoromethyl-4-quinolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1-Methyl-3-methylthiomethyl-7-trifluoromethyl-4-quinolone | HCID 12807842 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methyl-3-methylsulphinylmethyl-7-trifluoromethyl-4-quinolone | HCID 12807843 | — |
Reaction Steps
To a stirred solution of 1-methyl-3-methylthiomethyl-7-trifluoromethyl-4-quinolone (6.5 g.) in dichloromethane (150 ml.) at -10° was added a solution of 3-chloroperbenzoic acid (85%, 4.2 g.) in dichloromethane (90 ml.) during 30 minutes. The solution was extracted with saturated aqueous sodium bicarbonate until free of per-acid. The organic phase was dried over anhydrous magnesium sulphate and evaporated to give a solid product. This was crystallised from ethyl acetate:dichloromethane to give the novel 1-methyl-3-methylsulphinylmethyl-7-trifluoromethyl-4-quinolone, m.p. 208°-210°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04442109 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-90208ae83c3f4f1798f89d2c41f9da0c |
| Source note | uspto-grants-1984_04 |