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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275108Generated: November 1, 2026

Thionyl Chloride → HCID 13106290, compound

https://huagongshe.com/reaction/275108

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-methylethyl}-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 first dissolved and then began to 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 numberUS05391825
Source datasetuspto-grants-1995_02
ORD IDord-2eeb919c4cf7456988502e2b0d8d512f
Source noteuspto-grants-1995_02