1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one

Base Information

Chemical Name:1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one
CAS No.:1402048-59-2
Molecular Formula:C₄₁H₆₅NO₅S₂
Molecular Weight:716.103
Hs Code.:

Synonyms:1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one

Suppliers and Price of 1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one

There total 6 articles about 1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one 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: 44.0%

: 1402049-49-3
4-[4-[3,5-di-tert-butyl-4-(4-hydroxybutoxy)phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxyphenyl-sulfanyl)piperidin-1-yl]-4-oxobutyric acid methyl ester

: 1402048-59-2
1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one

Guidance literature:: 4-[4-[3,5-di-tert-butyl-4-(4-hydroxybutoxy)phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxyphenyl-sulfanyl)piperidin-1-yl]-4-oxobutyric acid methyl ester; With lithium borohydride; In tetrahydrofuran; for 3h;

With hydrogenchloride; In tetrahydrofuran; water;

Reference yield:

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

: 1402048-59-2
1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one

Guidance literature:: Multi-step reaction with 7 steps

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

2.1: potassium carbonate / N,N-dimethyl-formamide / 4.5 h / 85 °C

3.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 9 h / 20 °C

4.1: dimethylsulfide borane complex / tetrahydrofuran / 20 °C

5.1: isopropyl alcohol; potassium hydroxide / 85 °C

5.2: pH 6 / Acidic aqueous solution

6.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0.5 h

7.1: lithium borohydride / tetrahydrofuran / 3 h

With hydrogenchloride; lithium borohydride; lithium hydroxide monohydrate; dimethylsulfide borane complex; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; isopropyl alcohol; potassium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

Reference yield:

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

: 1402048-59-2
1-[4-[3,5-di-tert-butyl-4-(4-hydroxy-butoxy)-phenylsulfanyl]-4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidin-1-yl]-4-hydroxy-butan-1-one

Guidance literature:: Multi-step reaction with 7 steps

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

2.1: potassium carbonate / N,N-dimethyl-formamide / 4.5 h / 85 °C

3.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 9 h / 20 °C

4.1: dimethylsulfide borane complex / tetrahydrofuran / 20 °C

5.1: isopropyl alcohol; potassium hydroxide / 85 °C

5.2: pH 6 / Acidic aqueous solution

6.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0.5 h

7.1: lithium borohydride / tetrahydrofuran / 3 h

With hydrogenchloride; lithium borohydride; lithium hydroxide monohydrate; dimethylsulfide borane complex; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; isopropyl alcohol; potassium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;