4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1204331-08-7
Molecular Formula:C₁₉H₂₄F₃NO₄
Molecular Weight:387.399
Hs Code.:

Synonyms:4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester

There total 12 articles about 4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl 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: 100.0%

: 1204331-07-6
4-(4-methoxycarbonyl-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester

: 1204331-08-7
4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: 4-(4-methoxycarbonyl-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester; With lithium hydroxide monohydrate; In methanol; water; at 40 ℃;

With hydrogenchloride; In water; pH=5;
DOI:10.1021/jm300601d

Reference yield:

: 375853-82-0,286961-14-6
tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-1(2H)-pyridinecarboxylate

: 1204331-08-7
4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine; N,N-phenylbistrifluoromethane-sulfonimide / N,N-dimethyl-formamide / 20 °C

1.2: 0.5 h / 110 °C / Microwave irradiation

2.1: hydrogen; 10% Pd/C / ethanol / Inert atmosphere

3.1: lithium hydroxide monohydrate / methanol; water / 40 °C

3.2: pH 5

With N,N-phenylbistrifluoromethane-sulfonimide; lithium hydroxide monohydrate; 10% Pd/C; hydrogen; N-ethyl-N,N-diisopropylamine; In methanol; ethanol; water; N,N-dimethyl-formamide; 1.2: |Suzuki Coupling;
DOI:10.1021/jm300601d

Reference yield:

: 340158-54-5
4-hydroxy-5-iodo-2-methyl-benzoic acid methyl ester

: 1204331-08-7
4-(4-carboxy-5-methyl-2-trifluoromethylphenyl)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 80 °C

2.1: copper(l) iodide / 1-methyl-pyrrolidin-2-one / 5 h / 150 °C

3.1: hydrogen; 10% Pd/C / ethanol / Inert atmosphere

4.1: N-ethyl-N,N-diisopropylamine; N,N-phenylbistrifluoromethane-sulfonimide / N,N-dimethyl-formamide / 20 °C

4.2: 0.5 h / 110 °C / Microwave irradiation

5.1: hydrogen; 10% Pd/C / ethanol / Inert atmosphere

6.1: lithium hydroxide monohydrate / methanol; water / 40 °C

6.2: pH 5

With copper(l) iodide; N,N-phenylbistrifluoromethane-sulfonimide; lithium hydroxide monohydrate; 10% Pd/C; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; In 1-methyl-pyrrolidin-2-one; methanol; ethanol; water; N,N-dimethyl-formamide; 4.2: |Suzuki Coupling;
DOI:10.1021/jm300601d