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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834222Generated: November 2, 2026

Benzoyl chloride → HCID 21386590, compound

https://huagongshe.com/reaction/1834222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 21386605HCID 21386605—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 21386590HCID 21386590—

Reaction Steps

1 Milliliter of benzoyl chloride was added dropwise, while stirring and cooling with an ice mixture, to a solution of 1.4 g of 3-carbomethoxyamino-7-(3-trifluoromethyl-phenylsulfonyloxy)-1H-2,1,4-benzothiadiazine-S-oxide in 20 ml of pyridine. After the mixture has been stirred for 2 hours at 0° C, 1 ml of benzoyl chloride was added once more. After another hour of stirring at 0° C, the reaction mixture was diluted with water. It was then shaken with ethyl acetate, and the extract was washed with saturated sodium chloride solution. After evaporation of the solvent, the residue was isolated by trituration with methanol and filtration. 1-Benzoyl-3-carbomethoxyamino-7-(3-trifluoromethyl-phenylsulfonyloxy)-1H-2,1,4-benzothiadiazine-S-oxide was obtained in a yield of 1.1 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04069325
Source datasetuspto-grants-1978_01
ORD IDord-53ea3389edf8404ab79a97511399af25
Source noteuspto-grants-1978_01