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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567658Generated: October 25, 2026

1-Octene → Octane

https://huagongshe.com/reaction/567658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-OcteneHCID 8125—
CatalystBis(cyclopentadienyl)titanium(IV) chlorideHCID 416358—
SolventCyclohexaneHCID 8078—
SolventHeptaneHCID 8900—
ProductOctaneHCID 356—
ProductOct-2-eneHCID 8126—

Reaction Steps

0.12 mmoles of bis-(η5-cyclopentadienyl)titanium dichloride (Cp2TiCl2; Aldrich commercial product), 20 ml of anhydrous cyclohexane, 0.03 ml of a solution of n-dibutylglima 0.45 M in anhydrous cyclohexane and 0.54 ml of 1 molar Mg(butyl)2 in n-heptane (atomic ratio Mg/Ti=4.5), are charged into a tailed test-tube equipped with a magnetic stirrer, in an atmosphere of argon. The mixture is left under stirring for 20 hours at room temperature. 18.8 ml of 1-octene (distilled and maintained on molecular sieves) are added. At this point the solution is siphoned in an autoclave previously maintained under argon and the same procedure is carried out as described in example 1 above. At the end it is cooled to room temperature. About 14 ml of octane and 4 ml of 2-octene are obtained by distillation (GC, mass GC and NMR analyses). The results and process conditions are summarized in table 1 below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180553B2
Source datasetuspto-grants-2001_01
ORD IDord-eeb13e21c0b84dd1bbb2834d05d724ac
Source noteuspto-grants-2001_01