2-phenyl>carbamoyl>benzoic acid

Base Information

Chemical Name:2-phenyl>carbamoyl>benzoic acid
CAS No.:118683-79-7
Molecular Formula:C₂₆H₂₅NO₆
Molecular Weight:447.488
Hs Code.:

2-<N-<3-<(4-acetyl-3-hydroxy-2-propylphenoxy)methyl>phenyl>carbamoyl>benzoic acid

Synonyms:2-phenyl>carbamoyl>benzoic acid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-phenyl>carbamoyl>benzoic acid

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Technology Process of 2-phenyl>carbamoyl>benzoic acid

There total 6 articles about 2-phenyl>carbamoyl>benzoic 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: 87.0%

: 85-44-9
phthalic anhydride

: 104013-60-7
3-<(4-acetyl-3-hydroxy-2-propylphenoxy)methyl>aniline

: 118683-79-7
2-phenyl>carbamoyl>benzoic acid

Guidance literature:: With pyridine; In dichloromethane; for 2h; Ambient temperature;

Reference yield:

: 40786-69-4
1-(2,4-dihydroxy-3-propylphenyl)ethanone

: 118683-79-7
2-phenyl>carbamoyl>benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / K₂CO₃ / acetone / 12 h / Heating

2: 82 percent / CF₃CO₂H / CH₂Cl₂ / 1.5 h / Ambient temperature

3: 87 percent / pyridine / CH₂Cl₂ / 2 h / Ambient temperature

With pyridine; potassium carbonate; trifluoroacetic acid; In dichloromethane; acetone;

Reference yield:

: 1877-77-6
3-aminobenzenemethanol

: 118683-79-7
2-phenyl>carbamoyl>benzoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 78 percent / tetrahydrofuran / 5 h / Heating

2: 74 percent / CBr₄, Ph₃P / CH₂Cl₂ / 1.5 h / 0 °C

3: 92 percent / K₂CO₃ / acetone / 12 h / Heating

4: 82 percent / CF₃CO₂H / CH₂Cl₂ / 1.5 h / Ambient temperature

5: 87 percent / pyridine / CH₂Cl₂ / 2 h / Ambient temperature

With pyridine; carbon tetrabromide; potassium carbonate; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetone;