Production Method 1

581-42-0

496-11-7

573-98-8

527-53-7

569-41-5

575-41-7

65051-83-4

767-59-9

620-14-4

2131-42-2

4175-53-5

27133-93-3

5325-97-3

3296-50-2

493-02-7

2039-89-6

629-59-4

1120-21-4

22531-20-0

2234-75-5

Reaction Conditions

1.1 Reagents: Dodecane ,  Decane ,  Tridecane ,  Pentadecane ,  Hydrogen Catalysts: Ruthenium ;  134.1 bar; 3.25 h, 157.6 bar, rt → 305 °C

Reference

An improved catalytic pyrolysis concept for renewable aromatics from biomass involving a recycling strategy for co-produced polycyclic aromatic hydrocarbons

Genuino, Homer C.; Muizebelt, Inouk; Heeres, Andre; Schenk, Niels J.; Winkelman, Jos G. M.; et al, Green Chemistry, 2019, 21(14), 3802-3806

1H-Indene,2,3-dihydro-1,3-dimethyl- Raw materials

• 2,6-Dimethylnaphthalene
• Indane
• 1,2-Dimethylnaphthalene
• 1,2,3,5-Tetramethylbenzene
• 1,8-Dimethylnaphthalene
• 1,3-Dimethylnaphthalene
• Benzene,(1-methyl-2-cyclopropen-1-yl)-
• 1-Methyl-1H-indene
• 3-Ethyltoluene
• Naphthalene,1,4,6-trimethyl-

1H-Indene,2,3-dihydro-1,3-dimethyl- Preparation Products

• 1H-Indene,2,3-dihydromethyl- (27133-93-3)
• 1,2,3,4,5,6,7,8-Octahydrophenanthrene (>85%) (5325-97-3)
• 1H-Indene, octahydro-, trans- (3296-50-2)
• 1H-Indene,2,3-dihydro-1,3-dimethyl- (4175-53-5)
• trans-Decahydronaphthalene (493-02-7)
• 2,5-Dimethylstyrene (stabilized with 4-tert-butylcatechol) (2039-89-6)
• n-Tetradecane (629-59-4)
• Undecane (1120-21-4)
• Naphthalene,6-ethyl-1,2,3,4-tetrahydro- (22531-20-0)
• 1,2,4-Trimethylcyclohexane (2234-75-5)

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