[4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide

Base Information

Chemical Name:[4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide
CAS No.:1402048-64-9
Molecular Formula:C₃₆H₅₆N₂O₃S₂
Molecular Weight:628.984
Hs Code.:

Synonyms:[4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide

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Chemical Property of [4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide

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Technology Process of [4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide

There total 3 articles about [4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide 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: 73.0%

: 683-57-8
bromo-acetic acid amide

: 1402048-10-5
2,6-di-tert-butyl-4-[4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)-piperidin-4-ylsulfanyl]-phenol

: 1402048-64-9
[4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 18h;

Reference yield:

: 950-59-4
4-hydroxy-3,5-di-tert-butylthiophenol

: 1402048-64-9
[4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / methanol / 20 h / 45 °C

2.1: potassium tert-butylate / tetrahydrofuran / 5 h / Inert atmosphere; Reflux

3.1: isopropyl alcohol; potassium hydroxide / 18 h / Inert atmosphere; Reflux

3.2: 20 °C / pH ~ 6

4.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 18 h / 20 °C

With hydrogenchloride; potassium tert-butylate; N-ethyl-N,N-diisopropylamine; isopropyl alcohol; potassium hydroxide; In tetrahydrofuran; methanol;

Reference yield:

: 29976-53-2
N-ethoxycarbonyl-4-piperidone

: 1402048-64-9
[4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-(3,5-di-tert-butyl-4-methoxy-phenylsulfanyl)piperidin-1-yl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / methanol / 20 h / 45 °C

2.1: potassium tert-butylate / tetrahydrofuran / 5 h / Inert atmosphere; Reflux

3.1: isopropyl alcohol; potassium hydroxide / 18 h / Inert atmosphere; Reflux

3.2: 20 °C / pH ~ 6

4.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 18 h / 20 °C

With hydrogenchloride; potassium tert-butylate; N-ethyl-N,N-diisopropylamine; isopropyl alcohol; potassium hydroxide; In tetrahydrofuran; methanol;