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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41779Generated: October 25, 2026

2,3,5-Triiodobenzoic acid → 1-Decene

https://huagongshe.com/reaction/41779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,5-Triiodobenzoic acidHCID 6948—
Reactant1-DeceneHCID 13381—
ReactantHCID 178418361HCID 178418361—
SolventTolueneHCID 1140—
SolventHeptaneHCID 8900—
Product1-DeceneHCID 13381—
ProductDecaneHCID 15600—

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 100 g of purified 1-decene, 1.301 g of a TIBA stock solution (20 mg TIBA/g toluene solution) and 0.445 g of Metallocene A stock solution (1 mg Metallocene A/g toluene solution) was charged into a clean 600 ml autoclave equipped with an agitator, at room temperature. The reactor was then pressurized with 30 psig hydrogen. The mixture was then heated to 90° C. with stirring. A second solution made by adding a) 0.641 g of Activator A stock solution (1 mg Activator A/g toluene solution) and b) 20 g toluene solvent and was added and the reaction temperature was maintained at 90° C. overnight, then cooled down to room temperature, and any reactor pressure was vented. The liquid product was diluted with 50 ml heptane, stirred with 5 g activated alumina for half an hour and filtered to remove solids. The filtrate was analyzed by gas chromatography using an internal standard to obtain the wt % of normal-decane (n-C10) formation from 1-decene hydrogenation, wt % conversion to lubes and wt % lube yield. The lube product was then isolated by flashing the light ends (solvents, unreacted C10 fraction, and any fractions lighter than C30) and distilled at 180° C. under high vacuum (1 millitorr) for two hours to isolate the lube product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530712B2
Source datasetuspto-grants-2013_09
ORD IDord-70b03b60d66c4e9c88f474373cab2e3a
Source noteuspto-grants-2013_09