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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076753Generated: October 31, 2026

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

https://huagongshe.com/reaction/1076753

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 numberUS03957833
Source datasetuspto-grants-1976_05
ORD IDord-e49a58f6e15e4820bb11cd93762e16cf
Source noteuspto-grants-1976_05