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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253954Generated: October 26, 2026

2,6-Diisopropylnaphthalene → Naphthalene

https://huagongshe.com/reaction/2253954

Reaction equation

Participants

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

Reaction Steps

Naphthalene (80 g) and the catalyst from example 1 (4 g or 5% by weight on the naphthalene) are contacted with propylene at a temperature of 220° C. with an added pressure of propylene of 0.8×105Pa for 3 hours in a 300 ml Parr pressure autoclave operated under agitation. Analysis of the reaction mixture by gas chromatography gives a conversion of 89.0%, a yield in the 2,6-diisopropyl naphthalene of 34.4% and a yield in 2,7-diisopropyl naphthalene of 11.8%. The sum of the diisopropyl naphthalene represents 51.7% of the conversion. The selectivity to the 2,6-diisopropyl naphthalene is 38.7% and the selectivity to the 2,7-diisopropyl naphthalene is 13.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05233111
Source datasetuspto-grants-1993_08
ORD IDord-be31893a07f048138f6042a33214b228
Source noteuspto-grants-1993_08