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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981433Generated: October 27, 2026

Benzoyl chloride → 5-Amidino-2-benzoyloxybenzenesulfonic acid

https://huagongshe.com/reaction/1981433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant5-Amidino-2-hydroxybenzenesulfonic acidHCID 135598748—
SolventPyridineHCID 1049—
Product5-Amidino-2-benzoyloxybenzenesulfonic acidHCID 13178455—

Reaction Steps

To 30 ml of dried pyridine, was added 3.0 g of 5-amidino-2-hydroxybenzenesulfonic acid. To the mixture, while being cooled in ice, was slowly added dropwise 2.0 g of benzoyl chloride. After the addition, the mixture was stirred overnight at room temperature. The insolubles deposited from the reaction mixture were separated by filtration, washed with pyridine, then with water, finally with acetone, and suspended in methanol. The insolubles were removed by filtration, and ethyl ether was added to the filtrate to precipitate a colorless solid. The solid was collected by filtration and recrystallized from a methanol-ethyl ether mixture to obtain 5-amidino-2-benzoyloxybenzenesulfonic acid in colorless solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04514416
Source datasetuspto-grants-1985_04
ORD IDord-703e5952593c45aa8319c79932bf75bd
Source noteuspto-grants-1985_04