Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618865Generated: October 31, 2026

3,7,11-Trimethyl-6-dodecen-1-yn-3-ol → 1,6-Dodecadien-3-ol, 3,7,11-trimethyl-

https://huagongshe.com/reaction/618865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,7,11-Trimethyl-6-dodecen-1-yn-3-olHCID 53835752—
CatalystLindlars catalystHCID 131709914—
SolventHexaneHCID 8058—
Product1,6-Dodecadien-3-ol, 3,7,11-trimethyl-HCID 11583999.1%

Reaction Steps

An autoclave having an internal volume of 3 liters was charged with 630 g of the 3,7,11-trimethyl-6-dodecen -1-yn-3-ol thus obtained, 270 g of hexane and 0.22 g of a Lindlar catalyst (supported on calcium carbonate) to carry out the hydrogenation for 4 hours under hydrogen pressure of 5 to 8 kg/cm2 (gauge pressure) at a temperature of 25 to 43° C. Thereafter, the catalyst was filtered off, and the resultant filtrate was concentrated with a rotary evaporator to give 630 g of crude 3,7,11-trimethyl-1,6-dodecadien-3-ol. Analysis by gas chromatography (column: DC-550, available from Gasukuro Kogyo Inc.; column length: 3 m; column temperature: 160° C.; and column: PEG-20M, available from Gasukuro Kogyo Inc.; column length: 3 m; column temperature: 190° C.) revealed that the conversion of 3,7,11-trimethyl-6-dodecen-1-yn-3-ol was 95.5%, and the selectivity to 3,7,11-trimethyl -1,6-dodecadien-3-ol was 94.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05955636
Source datasetuspto-grants-1999_09
ORD IDord-cb0200cb47db47dcac9712f9c1f8646b
Source noteuspto-grants-1999_09