Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381899Generated: October 31, 2026

m-Chloroperbenzoic acid → 2-methoxy-5-methyl-2H-1,4-thiazin-3(4H)-one

https://huagongshe.com/reaction/1381899

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-Methyl-2h-1,4-thiazin-3(4h)-oneHCID 290017—
SolventMethanolHCID 887—
Product2-methoxy-5-methyl-2H-1,4-thiazin-3(4H)-oneHCID 1436979861.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804668
Source datasetuspto-grants-1989_02
ORD IDord-5a9e8f87d0e84e33951412dd4fb6b6b7
Source noteuspto-grants-1989_02