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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733695Generated: October 26, 2026

Triethylamine → 4-Oxo-3,4-dihydro-3-methanesulfonyloxy-1,2,3-benzotriazine

https://huagongshe.com/reaction/1733695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-hydroxy-1,2,3-benzotriazin-4(3H)-oneHCID 73026—
SolventBenzeneHCID 241—
Product4-Oxo-3,4-dihydro-3-methanesulfonyloxy-1,2,3-benzotriazineHCID 2189628173.3%

Reaction Steps

In benzene (30 ml) are dissolved 4-oxo-3,4-dihydro-3-hydroxy-1,2,3-benzotriazine (2.4 g) and triethylamine (2.1 ml) and thereto is added dropwise methanesulfonyl chloride (1.7 g), whereby faint exotherm occurs and crystals are precipitated. The reaction mixture is extracted with ethyl acetate (80 ml). The extract is washed with water, an aqueous sodium hydrogen carbonate and water in order, dried over anhydrous magnesium sulfate and then distilled to remove the solvent. The resulting residue is washed with ether-petroleum ether and dried to give 4-oxo-3,4-dihydro-3-methanesulfonyloxy-1,2,3-benzotriazine (2.6 g), melting point: 132°-134° C. Infrared spectrum: 1720, 1380, 1175 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242507
Source datasetuspto-grants-1980_12
ORD IDord-e6f1e57a0cc7492ea261fd8efefd6fc3
Source noteuspto-grants-1980_12