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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253955Generated: October 25, 2026

2,6-Diisopropylnaphthalene → Naphthalene

https://huagongshe.com/reaction/2253955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DiisopropylnaphthaleneHCID 32241—
Reactant1,2-DiisopropylnaphthaleneHCID 3023651—
Solvent2,7-DiisopropylnaphthaleneHCID 94505—
ProductNaphthaleneHCID 931—

Reaction Steps

Naphthalene (800 g) and the catalyst from example 2 (40 g or 5% by weight on the naphthalene) are contacted with propylene at a temperature of 250° C. with an added pressure of propylene of 0.8×105Pa for 1 hour 30 minutes in a 2 liter Parr pressure autoclave operated under agitation. Analysis of the reaction mixture by gas chromatography gives a conversion of 82.3%, a yield in the 2,6-diisopropyl naphthalene of 15.0% and a yield in 2,7-diisopropyl naphthalene of 9.4%. The sum of the diisopropyl naphthalene represents 32.5% of the conversion. The selectivity to the 2,6-diisopropyl naphthalene is 18.2% and the selectivity to the 2,7-diisopropyl naphthalene is 11.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05233111
Source datasetuspto-grants-1993_08
ORD IDord-a631472c3d6a48b889ab1aafa381aa49
Source noteuspto-grants-1993_08