Production Method 1

4373-67-5

79601-21-1

Reaction Conditions

Reference

3-Phenylpiperidines. Central dopamine-autoreceptor stimulating activity

Hacksell, Uli; Arvidsson, Lars Erik; Svensson, Uno; Nilsson, J. Lars G.; Sanchez, Domingo; et al, Journal of Medicinal Chemistry, 1981, 24(12), 1475-82

Production Method 2

1463888-26-7

79601-21-1

Reaction Conditions

1.1 Reagents: Trifluoroacetic acid Solvents: Dichloromethane ;  15 min, rt
1.2 Reagents: Sodium carbonate Solvents: Water ;  neutralized, rt

Reference

Cobalt-Catalyzed Cross-Coupling of 3- and 4-Iodopiperidines with Grignard Reagents

Gonnard, Laurine; Guerinot, Amandine; Cossy, Janine, Chemistry - A European Journal, 2015, 21(36), 12797-12803

Production Method 3

1463888-26-7

79601-21-1

Reaction Conditions

1.1 Reagents: Trifluoroacetic acid Solvents: Dichloromethane ;  1 h, rt
1.2 Reagents: Sodium carbonate Solvents: Water

Reference

Decarboxylative Negishi Coupling of Redox-Active Aliphatic Esters by Cobalt Catalysis

Liu, Xu-Ge; Zhou, Chu-Jun; Lin, E.; Han, Xiang-Lei; Zhang, Shang-Shi; et al, Angewandte Chemie, 2018, 57(40), 13096-13100

Production Method 4

88784-36-5

79601-21-1

Reaction Conditions

Reference

Enantiomers of substituted phenylazacycloalkanes

, United Kingdom, , ,

3-(3-Methoxyphenyl)piperidine Raw materials

• 3-(3-Methoxyphenyl)pyridine
• Piperidine, 3-(3-methoxyphenyl)-1-(phenylmethyl)-

3-(3-Methoxyphenyl)piperidine Preparation Products

• 3-(3-Methoxyphenyl)piperidine (79601-21-1)

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• 5. Dissolved oxygen sensor based on fluorescence quenching of oxygen-sensitive ruthenium complexes immobilized in sol–gel-derived porous silica coatings
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