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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072540Generated: November 4, 2026

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

https://huagongshe.com/reaction/2072540

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 (5hrs.) 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 numberUS04051319
Source datasetuspto-grants-1977_09
ORD IDord-8320d9c4ecb14bc99cff9898c37dab94
Source noteuspto-grants-1977_09