4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl ester

Base Information

Chemical Name:4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl ester
CAS No.:1602924-00-4
Molecular Formula:C₁₉H₂₃F₆NO₂
Molecular Weight:411.388
Hs Code.:

Synonyms:4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl ester

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Chemical Property of 4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl ester

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Technology Process of 4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl ester

There total 3 articles about 4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl 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: 48.0%

: 64321-45-5
3-(m-trifluoromethylphenyl)-piperidine

: 4,4,4-trifluoro-3-formyl-butyric acid ethyl ester

: 1602924-00-4
4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl ester

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane; at 20 ℃; for 13h; Inert atmosphere;

Reference yield:

: 328-62-1
4,4,4-trifluoro-3-(nitromethyl)butyric acid ethyl ester

: 1602924-00-4
4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide; water / tetrahydrofuran / 0.33 h / Inert atmosphere; Cooling with ice

1.2: 0.33 h / Inert atmosphere

2.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 13 h / 20 °C / Inert atmosphere

With water; sodium tris(acetoxy)borohydride; acetic acid; potassium hydroxide; In tetrahydrofuran; dichloromethane;

Reference yield:

: 25597-16-4
ethyl 4,4,4-trifluorocrotonate

: 1602924-00-4
4,4,4-trifluoro-3-[3-(3-trifluoromethyl-phenyl)-piperidin-1-ylmethyl]-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: N,N,N',N'-tetramethylguanidine / 13 h / 20 °C / Inert atmosphere

2.1: potassium hydroxide; water / tetrahydrofuran / 0.33 h / Inert atmosphere; Cooling with ice

2.2: 0.33 h / Inert atmosphere

3.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 13 h / 20 °C / Inert atmosphere

With water; sodium tris(acetoxy)borohydride; acetic acid; potassium hydroxide; N,N,N',N'-tetramethylguanidine; In tetrahydrofuran; dichloromethane;