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(2R,4S)-4-Methoxy-piperidine-2-carboxylic acid

Base Information Edit
  • Chemical Name:(2R,4S)-4-Methoxy-piperidine-2-carboxylic acid
  • CAS No.:135607-86-2
  • Molecular Formula:C7H13NO3
  • Molecular Weight:159.185
  • Hs Code.:
  • Mol file:135607-86-2.mol
(2R,4S)-4-Methoxy-piperidine-2-carboxylic acid

Synonyms:(2R,4S)-4-Methoxy-piperidine-2-carboxylic acid

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Chemical Property of (2R,4S)-4-Methoxy-piperidine-2-carboxylic acid Edit
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Technology Process of (2R,4S)-4-Methoxy-piperidine-2-carboxylic acid

There total 4 articles about (2R,4S)-4-Methoxy-piperidine-2-carboxylic acid 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:
With hydrogen; platinum(IV) oxide; In ethanol; water; at 60 ℃; for 24h; under 3102.9 Torr; Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1021/jo00289a058
Guidance literature:
Multi-step reaction with 4 steps
1: 30percent hydrogen peroxide / acetic acid / 24 h / Heating
2: dimethylcarbamyl chloride / CH2Cl2 / 24 h / Ambient temperature
3: 71 percent / 6 N HCl / 24 h / Heating
4: hydrogen / platinum oxide / ethanol; H2O / 24 h / 60 °C / 3102.9 Torr
With hydrogenchloride; hydrogen; dihydrogen peroxide; N,N-Dimethylcarbamoyl chloride; platinum(IV) oxide; In ethanol; dichloromethane; water; acetic acid;
DOI:10.1021/jo00289a058
Guidance literature:
Multi-step reaction with 3 steps
1: dimethylcarbamyl chloride / CH2Cl2 / 24 h / Ambient temperature
2: 71 percent / 6 N HCl / 24 h / Heating
3: hydrogen / platinum oxide / ethanol; H2O / 24 h / 60 °C / 3102.9 Torr
With hydrogenchloride; hydrogen; N,N-Dimethylcarbamoyl chloride; platinum(IV) oxide; In ethanol; dichloromethane; water;
DOI:10.1021/jo00289a058
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