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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758444Generated: November 3, 2026

Thionyl Chloride → HCID 13106290, compound

https://huagongshe.com/reaction/1758444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 13564370HCID 13564370—
SolventAcetonitrileHCID 6342—
ProductHCID 13106290HCID 1310629084.8%

Reaction Steps

In 1,000 ml of acetonitrile was suspended 17 g of 5-{2-[2-(2-ethoxyphenoxy)ethylamino]-1-hydroxy-2-methyl-ethyl}-2-methoxybenzenesulfonamide hydrochloride and while stirring the suspension, 9 g of thionyl chloride was added dropwise to the suspension at room temperature, whereby the product was dissolved and then began crystallize gradually. After stirring the mixture for two days, the crystals formed were recovered by filtration, washed with chloroform and dried to provide 15 g of 5-{1-chloro-2-[2-(2-ethoxyphenoxy)ethylamino]-2-methylethyl}-2-methoxybenzenesulfonamide hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04373106
Source datasetuspto-grants-1983_02
ORD IDord-8c03f68230634be788ecc8468afbb96f
Source noteuspto-grants-1983_02