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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106976Generated: October 26, 2026

Hydrochloric Acid → 10,12-Tricosadiynoic Acid

https://huagongshe.com/reaction/2106976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant10-Undecynoic acidHCID 31039—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant1-Iodododec-1-yneHCID 13600587—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthylamineHCID 6341—
Product10,12-Tricosadiynoic AcidHCID 538457—

Reaction Steps

10-Undecynoic acid (21.8 g, 0.120 mol) was neutralized with a solution of 57 mL 10 percent KOH in water and hydroxylamine hydrochloride (0.380 g) was added. Then a catalyst consisting of a solution of 1.9 g cuprous chloride in 16 g 70 percent aqueous ethylamine was added. A yellow precipitate formed immediately. A solution of the crude 1-iodo-1-dodecyne in 40 mL methanol was then added dropwise with stirring. The suspension was stirred for one hour after the addition. The reaction mixture was acidified by the addition of 2.5N HCl, filtered, and the filtrate and precipitate washed with ether. The ether layers were washed with water, thiosulfate solution, water and saturated sodium chloride. After drying Na2SO4) the solvents were removed under reduced pressure. The residue was induced to crystallize by scratching under petroleum ether. The crystals of the diyne acid (26.4 g, 74%) exhibited m.p. 57°-58° after recrystallization from acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933114
Source datasetuspto-grants-1990_06
ORD IDord-dea00503b4b24f5ab3f03420aaf878fd
Source noteuspto-grants-1990_06