2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol

Base Information

Chemical Name:2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol
CAS No.:1073186-73-8
Molecular Formula:C₂₅H₃₈N₂O₄S₂
Molecular Weight:494.72
Hs Code.:

Synonyms:2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol

Suppliers and Price of 2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol

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 2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol

There total 6 articles about 2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-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: 47.0%

: 1073186-99-8
5-[4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidine-1-sulfonyl]-1-methyl-1H-pyrrole-2-carboxylic acid methyl ester

: 1073186-73-8
2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol

Guidance literature:: 5-[4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidine-1-sulfonyl]-1-methyl-1H-pyrrole-2-carboxylic acid methyl ester; With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 2h;

With water; ammonium chloride; In tetrahydrofuran;

Reference yield:

: 109384-19-2
t-butyl 4-hydroxy piperidine-1-carboxylate

: 1073186-73-8
2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dichloromethane / 16.75 h / 0 - 20 °C

2.1: caesium carbonate / butanone / 8 h / 60 °C

2.2: 16.5 h / 20 °C

2.3: 0.5 h

3.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 5 h / 20 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 20 °C

With lithium aluminium tetrahydride; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; butanone;

Reference yield:

: 141699-59-4
1-(tert-butoxycarbonyl)piperidin-4-yl methanesulfonate

: 1073186-73-8
2,6-di-tert-butyl-4-[1-(5-hydroxymethyl-1-methyl-1H-pyrrole-2-sulfonyl)-piperidin-4-ylsulfanyl]-phenol

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / butanone / 8 h / 60 °C

1.2: 16.5 h / 20 °C

1.3: 0.5 h

2.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 5 h / 20 °C

3.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 20 °C

With lithium aluminium tetrahydride; caesium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; butanone;