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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380006Generated: November 2, 2026

p-Toluenesulfonic acid → 2-Methyl-2-(4-nitrophenyl)-1,3-dioxolane

https://huagongshe.com/reaction/1380006

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantp-NitroacetophenoneHCID 7487—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl orthoformateHCID 31214—
SolventEthylene GlycolHCID 174—
SolventDichloromethaneHCID 6344—
Product2-Methyl-2-(4-nitrophenyl)-1,3-dioxolaneHCID 606598—

Reaction Steps

P-Nitroacetophenone (1.65 g, 10 m mol), ethylene glycol (5 ml, 89 m mol), triethyl orthoformate (2.96 g, 20 m mol), and p-toluenesulfonic acid (0.086 g, 0.5 m mol) were combined in methylene chloride (4 ml). The solution was heated with an oil bath (50°-70° C., 6 hrs), cooled to room temperature, and poured into excess 10% sodium hydroxide solution. The phases were separated and the aqueous phase was extracted twice with methylene chloride. The combined organic phase was washed three times with water and dried with anhydrous sodium sulphate. Evaporation of the solvent left a light yellow product (1.78 g) with mp. 69°-71° C., (lit. 73°-75° C., see J. Pharm. Sci. 57, 784 (1968)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579679
Source datasetuspto-grants-1986_04
ORD IDord-63c671eb759f436fbbe69c307c68d7b5
Source noteuspto-grants-1986_04