tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate
CAS No.:1432674-49-1
Molecular Formula:C₁₇H₂₃F₂NO₃
Molecular Weight:327.371
Hs Code.:

Synonyms:tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate

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Technology Process of tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate

There total 3 articles about tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate 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: 66.0%

: 1432674-51-5
1-tert-butyl 3-methyl 3-fluoro-4-(4-fluorophenyl)piperidine-1,3-dicarboxylate

: 1432674-49-1
tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate

Guidance literature:: With lithium borohydride; In tetrahydrofuran; methanol; at 0 - 20 ℃; for 20.16h;

Reference yield:

: 205805-13-6
(±)-methyl 4β-(4-chlorophenyl)-1-methylpiperidine-3α-carboxylate

: 1432674-49-1
tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: carbonochloridic acid 1-chloro-ethyl ester / 1,2-dichloro-ethane / 4.5 h / 0 °C / Reflux

1.2: 48 h / Reflux

2.1: triethylamine / dichloromethane / 20 h / 20 °C

3.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / 0 °C

3.2: 0 - 20 °C

4.1: lithium borohydride / tetrahydrofuran; methanol / 20.16 h / 0 - 20 °C

With lithium borohydride; carbonochloridic acid 1-chloro-ethyl ester; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; 1,2-dichloro-ethane;

Reference yield:

: C₁₃H₁₆ClNO₂

: 1432674-49-1
tert-butyl 3-fluoro-4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / 20 h / 20 °C

2.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / 0 °C

2.2: 0 - 20 °C

3.1: lithium borohydride / tetrahydrofuran; methanol / 20.16 h / 0 - 20 °C

With lithium borohydride; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane;