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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065471Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 20540364, compound

https://huagongshe.com/reaction/1065471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium HydroxideHCID 14798—
Reactant2-(Bromomethyl)benzonitrileHCID 89599—
Reactant4-{2-[(3,3-Diphenylpropyl)amino]propyl}phenolHCID 13065281—
SolventWaterHCID 962—
ProductHCID 20540364HCID 20540364—

Reaction Steps

The mixture of 10.0 g 1-(4-hydroxyphenyl)-2-(3,3-diphenylpropylamino)-propane, 50 ml of dimethylsulfoxide and 2.4 g of sodium hydroxide in 10 ml of water is stirred at 60° for a half hour, whereupon 5.9 g of 2-cyanobenzyl bromide are added and the whole is stirred at room temperature for 20 hours. The mixture is diluted with water, extracted with ethyl acetate & the extract dried and evaporated. The residue is dissolved in the minimum amount of isopropanol, the solution neutralized with isopropanolic oxalic acid and the crude precipitate chromatographed on silica gel, using chloroform eluate, followed by chloroform-methanol (1:1). The initial fraction yields the 1-[4-(2-cyanobenzyloxy)-phenyl]-2-(3,3-diphenylpropylamino)-propane, showing I. R. bands at 2220 and 907 cm-1, and the second fraction the 1-[4-(2-carbamoylbenzyloxy)-phenyl]-2-(3,3-diphenylpropylamino)-propane, showing I. R. bands at 1655 and 1450 cm-1. The latter amide is taken up in aqueous ammonia, the mixture extracted with ethyl acetate & the extract dried and acidified with ethereal hydrogen chloride, to yield the corresponding hydrochloride melting at about 100° with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329367
Source datasetuspto-grants-1982_05
ORD IDord-bba93da0067e46abae7c1fcf1fb30de0
Source noteuspto-grants-1982_05