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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087122Generated: November 2, 2026

Hydrochloric Acid → HCID 15158834, compound

https://huagongshe.com/reaction/1087122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium HydroxideHCID 14798—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 15158833HCID 15158833—
SolventEthanolHCID 702—
ProductHCID 15158834HCID 15158834—

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of 4-[3-[[3-[[4-(acetyloxy)phenyl]thio]propyl]ethylamino] -2-hydroxypropoxy]-benzonitrile (3.80 g, 8.8 mmol) and toluene-4-sulfonic acid (1.67 g, 8.8 mmol) in ethanol (100 ml) was stirred and chilled to -15 ° C. To the chilled solution was added a solution of 3-chloroperbenzoic acid (2.05 g, 8.8 mmol) in ethanol (10 ml). The solution was stirred at room temperature for 2 h. Sodium hydroxide (8.8 g, 0.22 mol) was added and the solution was stirred for 1 h. The pH was adjusted to about 7 with hydrochloric acid. After evaporation the residue was treated with 2M hydrochloric acid and washed with diethylether. The acidic aqueous layer was treated with sodium hydroxide solution to pH =9 and extracted with three portions of ethyl acetate. The combined ethyl acetate fractions were dried over sodium sulfate and evaporated. The oily residue was purified by column chromatography on silica gel. Yield: 0.9 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034411
Source datasetuspto-grants-1991_07
ORD IDord-27b3256edafa4da794df101609851621
Source noteuspto-grants-1991_07