Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589489Generated: November 1, 2026

Pyridine → HCID 86740074, compound

https://huagongshe.com/reaction/1589489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 53931603HCID 53931603—
SolventDiethyl EtherHCID 3283—
ProductHCID 86740074HCID 86740074124.2%

Reaction Steps

To 30 ml of anhydrous pyridine, was added 2.7 g of 4-amidino-2-chlorophenol methanesulfonate. To the mixture, while being cooled in ice, was added 1.4 g of benzoyl chloride. The mixture was stirred for 30 minutes, while being cooled in ice, then for 5 hours at room temperature. The reaction mixture was mixed with 100 ml of ethyl ether to allow an oily substance to separate out. The oily substance was dissolved in 20 ml of methanol and poured into a saturated aqueous sodium hydrogencarbonate solution. The precipitated crystals were collected by filtration and washed with water, then with acetone. The washed crystals were added to 20 ml of methanol and admixed with 2.5 g of methanesulfonic acid. The insolubles were removed by filtration and 100 ml of ethyl ether was added to the filtrate. The precipitated colorless crystals were collected by filtration to obtain 2.5 g of 4-amidino-2-chlorophenyl benzoate methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04570006
Source datasetuspto-grants-1986_02
ORD IDord-e60fcfd0dd57450692dad69a494b7fe4
Source noteuspto-grants-1986_02