HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 2-methoxy-5-methyl-2H-1,4-thiazin-3(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-Methyl-2h-1,4-thiazin-3(4h)-one | HCID 290017 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-methoxy-5-methyl-2H-1,4-thiazin-3(4H)-one | HCID 14369798 | 61.1% |
Reaction Steps
m-Chloroperbenzoic acid (28.8 g) was added dropwise to a stirred solution of 5-methyl-2H-1,4-thiazin-3(4H)-one (15 g) in methanol (300 ml) under ice-cooling and the mixture was stirred at room temperature for 1 day. After the mixture was evaporated to dryness, the residue was extracted with ethyl acetate, washed with saturated sodium bicarbonate aqueous solution and dried over anhydrous magnesium sulfate. The solvent was evaporated to dryness to give 2-methoxy-5-methyl-2H-1,4-thiazin-3(4H)-one (11.3 g, yield 61%) as pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04804668 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-5a9e8f87d0e84e33951412dd4fb6b6b7 |
| Source note | uspto-grants-1989_02 |