Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

(2S,4R)-4-Ethyl-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester; compound with dicyclohexyl-amine

Base Information Edit
  • Chemical Name:(2S,4R)-4-Ethyl-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester; compound with dicyclohexyl-amine
  • CAS No.:123811-85-8
  • Molecular Formula:C12H23N*C13H23NO4
  • Molecular Weight:438.651
  • Hs Code.:
  • Mol file:123811-85-8.mol
(2S,4R)-4-Ethyl-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester; compound with dicyclohexyl-amine

Synonyms:

Suppliers and Price of (2S,4R)-4-Ethyl-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester; compound with dicyclohexyl-amine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 0 raw suppliers
Chemical Property of (2S,4R)-4-Ethyl-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester; compound with dicyclohexyl-amine Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (2S,4R)-4-Ethyl-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester; compound with dicyclohexyl-amine

There total 5 articles about (2S,4R)-4-Ethyl-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester; compound with dicyclohexyl-amine 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:
Multi-step reaction with 5 steps
1: 98 percent / dimethylcarbamyl chloride / CH2Cl2 / 24 h / Ambient temperature
2: 61 percent / 6 N HCl / 24 h / Heating
3: 100 percent / hydrogen / platinum oxide / ethanol; H2O / 24 h / 60 °C / 3102.9 Torr
4: 2 N NaOH / 2-methyl-propan-2-ol / 24 h / Ambient temperature; pH at 9.5
5: diethyl ether / 4 h
With hydrogenchloride; sodium hydroxide; hydrogen; N,N-Dimethylcarbamoyl chloride; platinum(IV) oxide; In diethyl ether; ethanol; dichloromethane; water; tert-butyl alcohol;
DOI:10.1021/jo00289a058
Guidance literature:
Multi-step reaction with 4 steps
1: 61 percent / 6 N HCl / 24 h / Heating
2: 100 percent / hydrogen / platinum oxide / ethanol; H2O / 24 h / 60 °C / 3102.9 Torr
3: 2 N NaOH / 2-methyl-propan-2-ol / 24 h / Ambient temperature; pH at 9.5
4: diethyl ether / 4 h
With hydrogenchloride; sodium hydroxide; hydrogen; platinum(IV) oxide; In diethyl ether; ethanol; water; tert-butyl alcohol;
DOI:10.1021/jo00289a058
Guidance literature:
Multi-step reaction with 3 steps
1: 100 percent / hydrogen / platinum oxide / ethanol; H2O / 24 h / 60 °C / 3102.9 Torr
2: 2 N NaOH / 2-methyl-propan-2-ol / 24 h / Ambient temperature; pH at 9.5
3: diethyl ether / 4 h
With sodium hydroxide; hydrogen; platinum(IV) oxide; In diethyl ether; ethanol; water; tert-butyl alcohol;
DOI:10.1021/jo00289a058
Post RFQ for Price