4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic acid

Base Information

Chemical Name:4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic acid
CAS No.:1369958-16-6
Molecular Formula:C₂₅H₂₅NO₆S
Molecular Weight:467.543
Hs Code.:

Synonyms:4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic acid

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Chemical Property of 4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic acid

Chemical Property:

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Technology Process of 4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic acid

There total 5 articles about 4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic 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:

: 1369958-18-8
ethyl 4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoate

: 1369958-16-6
4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic acid

Guidance literature:: With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 1h;

Reference yield:

: 1849-36-1
para-nitrobenzenethiol

: 1369958-16-6
4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic acid

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / dichloromethane / 5 h / 20 °C / Cooling with ice; Inert atmosphere

2: 3-chloro-benzenecarboperoxoic acid / chloroform / 1 h / 20 °C / Cooling with ice

3: potassium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 4 h / 50 °C / Inert atmosphere

4: tin(ll) chloride / ethyl acetate / 2 h / 80 °C

5: pyridine / Dichlorodifluoromethane / 0 °C / Inert atmosphere

6: water; lithium hydroxide / tetrahydrofuran; methanol / 1 h / 20 °C

With pyridine; water; tetra-(n-butyl)ammonium iodide; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; tin(ll) chloride; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; chloroform; Dichlorodifluoromethane; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 1369958-15-5
ethyl 4-(benzyloxy)-2-[(4-nitrophenyl)sulfonyl]butanoate

: 1369958-16-6
4-(benzyloxy)-2-[(4-{[(4-methylphenyl)carbonyl]amino}phenyl)sulfonyl]butanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: tin(ll) chloride / ethyl acetate / 2 h / 80 °C

2: pyridine / Dichlorodifluoromethane / 0 °C / Inert atmosphere

3: water; lithium hydroxide / tetrahydrofuran; methanol / 1 h / 20 °C

With pyridine; water; tin(ll) chloride; lithium hydroxide; In tetrahydrofuran; methanol; Dichlorodifluoromethane; ethyl acetate;