Production Method 1

9005-53-2

219726-60-0

103-81-1

831-00-5

60826-26-8

2219-78-5

74421-05-9

22607-11-0

94391-24-9

7443-70-1

51504-54-2

72386-20-0

79-31-2

494-99-5

646-07-1

4041-09-2

1131-62-0

432-25-7

56687-68-4

93-15-2

Reaction Conditions

1.1 Reagents: Sodium hydroxide Catalysts: Molybdenum ,  Copper Solvents: Methanol ,  Water ;  7 h, 220 °C
1.2 Reagents: Water

Reference

Cu-Mo doped zeolite ZSM-5 catalyzed conversion of lignin to alkyl phenols with high selectivity

Singh, Sunit Kumar; et al, Catalysis Science & Technology, 2015, 5(4), 2117-2124

Cyclopentane, 1-ethyl-2-(4-methylpentyl)- Raw materials

• Lignin

Cyclopentane, 1-ethyl-2-(4-methylpentyl)- Preparation Products

• 2-Phenylacetamide (103-81-1)
• 2',4'-Dimethoxypropiophenone (831-00-5)
• 3-Acetoxydodecane (60826-26-8)
• Phenol,2-ethyl-4,5-dimethyl- (2219-78-5)
• 2,4-heptadiene, 2,4-dimethyl- (74421-05-9)
• 2,5-Dimethyl-3,4-hexanediol (22607-11-0)
• 2-Cyclohexen-1-one, 3-acetyl-2,4,4-trimethyl- (94391-24-9)
• Cyclopentane, 1-ethyl-2-(4-methylpentyl)- (219726-60-0)
• cis-2-Methylcyclohexanol (7443-70-1)
• 2,3,4,5-Tetramethyl-1,4-hexadiene (51504-54-2)
• 2-Ethyl-5-propylphenol (72386-20-0)
• 2-Methylpropanoic acid (79-31-2)
• 3,4-Dimethoxytoluene (494-99-5)
• 4-Methylpentanoic acid (646-07-1)
• 2,5-dimethylcyclopentan-1-one (4041-09-2)
• 3',4'-Dimethoxyacetophenone (1131-62-0)
• β-Cyclocitral (432-25-7)
• [1,1'-Bicyclopropyl]-2-octanoic acid, 2'-hexyl-, methyl ester (56687-68-4)
• Methyl Eugenol (93-15-2)

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