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(2R,6R)-1,2-Dibenzyl-piperidine-2,6-dicarboxylic acid dimethyl ester

Base Information Edit
  • Chemical Name:(2R,6R)-1,2-Dibenzyl-piperidine-2,6-dicarboxylic acid dimethyl ester
  • CAS No.:246031-44-7
  • Molecular Formula:C23H27NO4
  • Molecular Weight:381.472
  • Hs Code.:
  • Mol file:246031-44-7.mol
(2R,6R)-1,2-Dibenzyl-piperidine-2,6-dicarboxylic acid dimethyl ester

Synonyms:(2R,6R)-1,2-Dibenzyl-piperidine-2,6-dicarboxylic acid dimethyl ester

Suppliers and Price of (2R,6R)-1,2-Dibenzyl-piperidine-2,6-dicarboxylic acid dimethyl ester
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Chemical Property of (2R,6R)-1,2-Dibenzyl-piperidine-2,6-dicarboxylic acid dimethyl ester Edit
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Technology Process of (2R,6R)-1,2-Dibenzyl-piperidine-2,6-dicarboxylic acid dimethyl ester

There total 4 articles about (2R,6R)-1,2-Dibenzyl-piperidine-2,6-dicarboxylic acid dimethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Dimethyl cis-N-benzyl-2,6-piperidinedicarboxylate; With chiral bis-lithium amide base; In tetrahydrofuran; at -78 ℃; for 1h;
benzyl bromide; In tetrahydrofuran; at -78 - 20 ℃;
DOI:10.1055/s-1999-2813
Guidance literature:
Multi-step reaction with 3 steps
1.1: 91 percent / H2 / Pd/C / ethanol / 10343 Torr
2.1: 86 percent / Na2CO3; H2O / CH2Cl2
3.1: chiral bis-lithium amide base / tetrahydrofuran / 1 h / -78 °C
3.2: 78 percent / tetrahydrofuran / -78 - 20 °C
With chiral bis-lithium amide base; water; hydrogen; sodium carbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; 1.1: Catalytic hydrogenation / 2.1: Alkylation / 3.1: Metallation / 3.2: Alkylation;
DOI:10.1055/s-1999-2813
Guidance literature:
Multi-step reaction with 4 steps
1.1: 75 percent / 2,2-dimethoxypropane; HCl
2.1: 91 percent / H2 / Pd/C / ethanol / 10343 Torr
3.1: 86 percent / Na2CO3; H2O / CH2Cl2
4.1: chiral bis-lithium amide base / tetrahydrofuran / 1 h / -78 °C
4.2: 78 percent / tetrahydrofuran / -78 - 20 °C
With hydrogenchloride; chiral bis-lithium amide base; water; hydrogen; sodium carbonate; 2,2-dimethoxy-propane; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; 1.1: Esterification / 2.1: Catalytic hydrogenation / 3.1: Alkylation / 4.1: Metallation / 4.2: Alkylation;
DOI:10.1055/s-1999-2813
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