1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone

Base Information

Chemical Name:1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone
CAS No.:1402048-07-0
Molecular Formula:C₄₂H₆₆N₂O₄S₂
Molecular Weight:727.129
Hs Code.:

1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone

Synonyms:1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone

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Chemical Property of 1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone

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Technology Process of 1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone

There total 4 articles about 1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone 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:

: 123-75-1
pyrrolidine

: 1402049-16-4
2-chloro-1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-ethanone

: 1402048-07-0
1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone

Guidance literature:: In tetrahydrofuran; at 55 ℃; for 2h;

Reference yield:

: 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

: 1402048-07-0
1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone

Guidance literature:: Multi-step reaction with 3 steps

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

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.5 h / 20 °C

3: tetrahydrofuran / 2 h / 55 °C

With 2-methoxy-ethanol; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran;

Reference yield:

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

: 1402048-07-0
1-{4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidin-1-yl}-2-pyrrolidin-1-yl-ethanone

Guidance literature:: Multi-step reaction with 5 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

4: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.5 h / 20 °C

5: tetrahydrofuran / 2 h / 55 °C

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