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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885670Generated: October 25, 2026

6-(Hydroxymethyl)-2H-benzo[b][1,4]thiazin-3(4H)-one → 3-Oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carbaldehyde

https://huagongshe.com/reaction/885670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Hydroxymethyl)-2H-benzo[b][1,4]thiazin-3(4H)-oneHCID 21873700—
CatalystManganese dioxideHCID 14801—
SolventChloroform tetrahydrofuranHCID 21956068—
Product3-Oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carbaldehydeHCID 1094334857.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 6-hydroxymethyl-4H-benzo[1,4]thiazin-3-one (360 mg, 1.8 mmol) in THF/CHCl3 (2:1, 18 mL) was added MnO2 (1.6 g, 18 mmol) and the resulting suspension was heated to 70° C. and stirred for 4 h. The suspension was filtered through diatomaceous earth and the filtrate was concentrated. The resulting solid was triturated with EtOAc/hexanes (1:1) and a minimal amount of CH3OH to provide 200 mg (56%) of the title compound as a tan solid. MS (ESI): exact mass calculated for C9H7NO2S, 193.02; m/z found, 194.1 [M+H]+. 1H NMR (500 MHz, CDCl3): 9.94 (s, 1H), 8.78 (br s, 1H), 7.54-7.49 (m, 2H), 7.37 (d, J=1.5, 1H), 3.52 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242275B2
Source datasetuspto-grants-2012_08
ORD IDord-5d82461db8b34ae2b2f094a93fd85335
Source noteuspto-grants-2012_08