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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283518Generated: October 25, 2026

Hexanal → 3-Decyn-5-ol

https://huagongshe.com/reaction/1283518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexanalHCID 6184—
Reactant1,3-ButadieneHCID 7845—
Reactant1-ButyneHCID 7846—
ReactantDimethylacetyleneHCID 10419—
Reactant1,2-ButadieneHCID 11535—
SolventTetrahydrofuranHCID 8028—
Product3-Decyn-5-olHCID 21518441—

Reaction Steps

Following the procedure of Example 1, but with a pressure equalizing dropping funnel in place of the gas addition tube, 5.2 g. of lithium metal powder and 125 ml. of tetrahydrofuran are added to the flask. 65 g. of ammonia gas is condensed into the slurry with stirring forming a liquid-copper-gold colored lithium ammonia adduct. 190 g. of a mixture containing about 18% 1,2-butadiene, 21% 1,3-butadiene, 4% 1-butyne, 3.3% 2-butyne and about 25% isomeric butenes dissolved in 800 ml. tetrahydrofuran was added over a 70 minute period with stirring while maintaining the temperature at about 50°C. to 60°C. The mixture was refluxed to drive off excess gases and cooled. An aliquot of the product was reacted with 1-hexanal producing 3-decyn-5-ol which by gas chromotograph analysis, establishes a yield of butynyllithium in excess of 90%, based on lithium.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975453
Source datasetuspto-grants-1976_08
ORD IDord-a28dd0458317429e893d593529ac2648
Source noteuspto-grants-1976_08