Production Method 1

493-02-7

529-32-8

825-51-4

21370-71-8

16021-08-2

55693-34-0

Reaction Conditions

1.1 Reagents: Trifluoroacetic acid ,  2,2′-Bipyridine ,  Oxygen Catalysts: Hexakis[μ-(acetato-κO:κO′)]-μ3-oxotris(pyridine)triiron Solvents: Pyridine

Reference

Selective oxidation of saturated hydrocarbons using an electrochemical modification of the Gif system

Balavoine, Gilbert; et al, Tetrahedron Letters, 1986, 27(25), 2849-52

Production Method 2

529-32-8

825-51-4

3574-58-1

4832-17-1

4832-16-0

1654-87-1

Reaction Conditions

1.1 Reagents: Oxygen Catalysts: Carbon Solvents: Acetone ;  2 h, 3 MPa, 150 °C

Reference

Continuous Homogeneous Catalytic Oxidation of C-H Bonds by Metal-Free Carbon Dots with a Poly(ascorbic acid) Structure

Wang, Xiao; et al, ACS Applied Materials & Interfaces, 2022, 14(23), 26682-26689

decahydronaphthalen-1-ol Raw materials

• trans-Decahydronaphthalene

decahydronaphthalen-1-ol Preparation Products

• decahydronaphthalen-2-ol (825-51-4)
• trans-1-Decalone (21370-71-8)
• 4a(2H)-Naphthalenol,octahydro-, cis- (3574-58-1)
• 3,4,4a,5,6,7,8,8a-octahydro-1h-naphthalen-2-one (4832-17-1)
• 2(1H)-Naphthalenone,octahydro-, (4aR,8aR)-rel- (16021-08-2)
• octahydronaphthalen-1(2H)-one (4832-16-0)
• 4a(2H)-Naphthalenol,octahydro-, trans- (1654-87-1)
• decahydronaphthalen-1-ol (529-32-8)
• 4a(2H)-Naphthalenol,octahydro- (55693-34-0)

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• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Cyclic alcohols and derivatives
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Alcohols and polyols Cyclic alcohols and derivatives

• 2216-51-5(L(-)-Menthol)
• 700-57-2(2-Adamantanol)
• 1490-04-6(Menthol)
• 20601-38-1(4,4'-Bicyclohexanol)
• 14648-57-8(2-Ethyl-2-adamantanol)
• 4534-74-1(trans-4-Ethylcyclohexanol)
• 16844-71-6(Epifriedelanol)
• 589-91-3(4-methylcyclohexan-1-ol)
• 702-98-7(2-Methyl-2-adamantanol)
• 52204-65-6(4-Propylcyclohexanol)