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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390402Generated: October 30, 2026

p-Toluenesulfonic acid → p-[(1,5-Dimethylhexyl)oxy]benzoic acid propargyl ester

https://huagongshe.com/reaction/1390402

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPropargyl alcoholHCID 7859—
ReactantHCID 54404637HCID 54404637—
Productp-[(1,5-Dimethylhexyl)oxy]benzoic acid propargyl esterHCID 53978508—

Reaction Steps

13 g of p-[(1,5-dimethylhexyl)oxy]benzoic acid methyl ester is heated to reflux with 9 g of propargyl alcohol and 0.1 g of p-toluenesulphonic acid. The excess propargyl alcohol is thereupon slowly (5 hrs.) distilled off. The residue is poured onto water and extracted with diethyl ether. The ether phase is dried with sodium sulfate and evaporated. There is obtained dark-yellow p-[(1,5-dimethylhexyl)oxy]benzoic acid propargyl ester which is purified on Kieselgel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138579
Source datasetuspto-grants-1979_02
ORD IDord-7e44eb09f9e54fe7ab797be45c72927f
Source noteuspto-grants-1979_02