1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid

Base Information

• Chemical Name: 1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid
• CAS No.: 226397-27-9
• Molecular Formula: C₂₁H₂₅NO₆S
• Molecular Weight: 419.499
• Mol file: 226397-27-9.mol

Synonyms:1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid

Chemical Property of 1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid

There total 6 articles about 1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-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:

Reference yield: 100.0%

1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester (226397-26-8) → 1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid (226397-27-9)

Guidance literature:

With sodium hydroxide; In tetrahydrofuran; ethanol; for 12h; Heating;

DOI:10.1021/jm0500875

Reference yield:

1-tert-butyl 4-ethyl 4-[(4-phenoxyphenyl)thio]piperidine-1,4-dicarboxylate (226396-40-3) → 1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid (226397-27-9)

Guidance literature:

Multi-step reaction with 4 steps

1: 87 percent / 3-chloroperbenzoic acid / CH₂Cl₂ / 1.5 h / 0 - 20 °C

2: 100 percent / HCl(gas) / ethyl acetate / 0.08 h

3: 100 percent / K₂CO₃ / dimethylformamide / 18 h / 20 °C

4: 100 percent / aq. NaOH / ethanol; tetrahydrofuran / 12 h / Heating

With hydrogenchloride; sodium hydroxide; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;

DOI:10.1021/jm0500875

Reference yield:

1-tert-butyl 4-ethyl 4-[(4-phenoxyphenyl)sulfonyl]piperidine-1,4-dicarboxylate (226396-42-5) → 1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid (226397-27-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 100 percent / HCl(gas) / ethyl acetate / 0.08 h

2: 100 percent / K₂CO₃ / dimethylformamide / 18 h / 20 °C

3: 100 percent / aq. NaOH / ethanol; tetrahydrofuran / 12 h / Heating

With hydrogenchloride; sodium hydroxide; potassium carbonate; In tetrahydrofuran; ethanol; ethyl acetate; N,N-dimethyl-formamide;

DOI:10.1021/jm0500875

upstream raw materials:

1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester

1-tert-butyl 4-ethyl 4-[(4-phenoxyphenyl)thio]piperidine-1,4-dicarboxylate

1-tert-butyl 4-ethyl 4-[(4-phenoxyphenyl)sulfonyl]piperidine-1,4-dicarboxylate

1,2-bis(4-phenoxyphenyl)disulfane

Downstream raw materials:

1-(2-methoxy-ethyl)-4-(4-phenoxy-benzenesulfonyl)-piperidine-4-carboxylic acid (tetrahydro-pyran-2-yloxy)-amide