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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414269Generated: November 4, 2026

Hydrochloric Acid → HCID 86734351, compound

https://huagongshe.com/reaction/1414269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantChlorineHCID 24526—
ReactantHCID 86734352HCID 86734352—
SolventCarbon TetrachlorideHCID 5943—
SolventChloroformHCID 6212—
ProductHCID 86734351HCID 86734351—

Reaction Steps

N-(2-Diethylaminoethyl)-4'-(β-phenylstyryl)butanesulfonanilide hydrochloride (10.5 g., 0.02 mole, refer to Procedure 51) is dissolved in a mixture of 300 ml. of carbon tetrachloride and 20 ml. of chloroform. The mixture is stirred and 39 ml. of a carbon tetrachloride solution containing 1.4 g. (0.02 mole) of chlorine is added thereto during 30 min. The mixture is kept at room temperature for an additional 30 min. and then refluxed for 1 hr. Vigorous evolution of hydrogen chloride gas is apparent during this period. The reaction mixture is allowed to cool and then neutralized with 100 ml. of aqueous 5% sodium hydroxide. The organic layer is separated, dried over magensium sulfate, and the solvent evaporated yielding 11.0 g. of the desired product. The material is purified by chromatography on an alumina column having dimensions 1 inch by 15 inches and eluting sequentially with 1:1 benzene-octane; benzene; benzene-chloroform, and finally with chloroform and collecting the eluate in 20 fractions. Fractions 15-19 are combined and the desired product recovered as the citrate salt, m.p. 65°-70°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001229
Source datasetuspto-grants-1977_01
ORD IDord-1f0c3439130942db8a7aac8d01da6ca7
Source noteuspto-grants-1977_01