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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977523Generated: October 27, 2026

3,7-Dimethyl-1-octyn-3-ol → 3,7-Dimethyloct-1-en-3-ol

https://huagongshe.com/reaction/1977523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,7-Dimethyl-1-octyn-3-olHCID 9812829—
CatalystLindlars catalystHCID 131709914—
SolventHexaneHCID 8058—
Product3,7-Dimethyloct-1-en-3-olHCID 86748—

Reaction Steps

An autoclave having an internal volume of 3 liters was charged with 1,140 g of the hexane solution containing 3,7-dimethyl-1-octyn-3-ol thus obtained and 0.27 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 crude 3,7-dimethyl-1-octen-3-ol. Above the procedures for the hydrogenation of 3,7-dimethyl-1-octyn-3-ol were repeated once more to obtain, in total, 1,590 g of crude 3,7-dimethyl-1-octen-3-ol. Analysis by gas chromatography (column: DC-550, available from Gasukuro Kogyo Inc.; column length: 3 m; column temperature: 100° C.; and column: PEG-HT, available from Gasukuro Kogyo Inc.; column length: 3 m; column temperature: 130° C.) revealed that the conversions of 3,7-dimethyl-1-octyn-3-ol were 99.7% and 97.3% for the respective runsof the hydrogenation, and the selectivities to 3,7-dimethyl-1-octen-3-ol were 95.0% and 95.8%, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232506B1
Source datasetuspto-grants-2001_05
ORD IDord-bb1a119cabe6495a88441aca97652bad
Source noteuspto-grants-2001_05