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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460283Generated: October 26, 2026

Propargyl alcohol → 3-Pentadecyl-1-(2-propynyloxy)benzene

https://huagongshe.com/reaction/1460283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantTriphenylphosphineHCID 11776—
ReactantHydrogenated cardanolHCID 68146—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product3-Pentadecyl-1-(2-propynyloxy)benzeneHCID 15045667—

Reaction Steps

To a solution of 24.4 g (80 mmol) of 3-pentadecylphenol, 4.93 g (88 mmol) of propargyl alcohol and 23.1 g (88 mmol) of triphenylphosphine cooled to 15° C. is added dropwise 15.3 g (13.9 ml, 88 mmol) of diethyl azodicarboxylate. The mixture is stirred for 4.5 hours and then is diluted with water and extracted with hexane (3 times). The hexane extracts are combined, washed with 1N sodium hydroxide and are dried over magnesium sulfate overnight. Filtration and evaporation gives crude oil which is subjected to flash chromatography using hexane as eluting solvent. The appropriate fractions are combined to give the title compound as an oil which solidifies upon standing: mp. 26°-27° C. The product is used without further characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05070207
Source datasetuspto-grants-1991_12
ORD IDord-d6b9cf94a0484c3b9e6002f1a161c67e
Source noteuspto-grants-1991_12