2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester

Base Information

Chemical Name:2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester
CAS No.:1195945-16-4
Molecular Formula:C₂₈H₂₆F₃NO₄
Molecular Weight:497.514
Hs Code.:

Synonyms:2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester

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Chemical Property of 2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester

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Technology Process of 2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester

There total 5 articles about 2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester 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:

: C₁₉H₁₆F₃NO₄

: 1875-89-4
2-(3-methylphenyl)ethanol

: 1195945-16-4
2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester

Guidance literature:: C₁₉H₁₆F₃NO₄; 2-(3-methylphenyl)ethanol; With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; Cooling with ice;

With hydrogenchloride; In methanol; water;

Reference yield:

: 1195945-14-2
3-acetoxy-4-trifluoromethyl-benzoic acid

: 1195945-16-4
2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 0.5 h / 20 °C

2: sodium hydrogencarbonate / dichloromethane; water / 0 °C

3: methanol; potassium carbonate

4: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / Cooling with ice

With methanol; oxalyl dichloride; di-isopropyl azodicarboxylate; sodium hydrogencarbonate; potassium carbonate; triphenylphosphine; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane; water;

Reference yield:

: 126541-87-5
3-hydroxy-4-trifluoromethylbenzoic acid

: 1195945-16-4
2-[3-(2-m-tolyl-ethoxy)-4-trifluoromethyl-benzoylamino]-indane-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 3 h / Reflux

1.2: 0.17 h / Reflux

2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 0.5 h / 20 °C

3.1: sodium hydrogencarbonate / dichloromethane; water / 0 °C

4.1: methanol; potassium carbonate

5.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / Cooling with ice

With methanol; oxalyl dichloride; di-isopropyl azodicarboxylate; sodium hydrogencarbonate; potassium carbonate; triphenylphosphine; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane; water;