2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol

Base Information

Chemical Name:2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol
CAS No.:1402047-98-6
Molecular Formula:C₃₆H₅₇NO₃S₂
Molecular Weight:615.985
Hs Code.:

Synonyms:2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol

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Chemical Property of 2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol

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Technology Process of 2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol

There total 4 articles about 2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol 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: 16.0%

: 1402047-97-5
4-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)phenylsulfanyl]piperidine-1-carboxylic acid ethyl ester

: 1402047-98-6
2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol

Guidance literature:: With 2-methoxy-ethanol; sodium hydroxide; at 120 ℃; for 18h;

Reference yield:

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

: 1402047-98-6
2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol

Guidance literature:: Multi-step reaction with 3 steps

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

2: potassium carbonate / N,N-dimethyl-formamide / 6 h / 85 °C

3: sodium hydroxide; 2-methoxy-ethanol / 18 h / 120 °C

With hydrogenchloride; 2-methoxy-ethanol; potassium carbonate; sodium hydroxide; In methanol; N,N-dimethyl-formamide;

Reference yield:

: 1402049-10-8
4,4-bis-(3,5-di-tert-butyl-4-hydroxyphenylsulfanyl)piperidine-1-carboxylic acid ethyl ester

: 1402047-98-6
2,6-di-tert-butyl-4-{4-[3,5-di-tert-butyl-4-(3-hydroxypropoxy)phenylsulfanyl]-piperidin-4-ylsulfanyl}phenol

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 85 °C

2: sodium hydroxide; 2-methoxy-ethanol / 18 h / 120 °C

With 2-methoxy-ethanol; potassium carbonate; sodium hydroxide; In N,N-dimethyl-formamide;