N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide

Base Information

• Chemical Name: N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide
• CAS No.: 862115-11-5
• Molecular Formula: C₂₂H₃₅NO₃S
• Molecular Weight: 393.591
• Mol file: 862115-11-5.mol

Synonyms:N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide

Chemical Property of N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide

There total 3 articles about N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide 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: 75.0%

6-tert-butyl-1-(toluene-4-sulfonyl)-1-aza-spiro[2.5]octane (862115-10-4) + 3-hydroxy-2-methyl-1-propene (513-42-8) → N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide (862115-11-5)

Guidance literature:

3-hydroxy-2-methyl-1-propene; With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; In diethyl ether; at 0 - 20 ℃; for 2h;

With magnesium bromide; In diethyl ether; at 0 - 20 ℃;

6-tert-butyl-1-(toluene-4-sulfonyl)-1-aza-spiro[2.5]octane; In diethyl ether; at 25 ℃; for 2h;

DOI:10.1021/ol050965t

Reference yield:

1-tert-butyl-4-methylenecyclohexane (13294-73-0) → N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide (862115-11-5)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 34 percent / N-bromosuccinimide / 7 / 20 °C

2.1: BuLi; TMEDA / diethyl ether / 2 h / 0 - 20 °C

2.2: MgBr₂ / diethyl ether / 0 - 20 °C

2.3: 75 percent / diethyl ether / 2 h / 25 °C

With N-Bromosuccinimide; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; 7; In diethyl ether;

DOI:10.1021/ol050965t

Reference yield:

chloroamine-T (127-65-1) → N-[4-tert-butyl-1-(3-hydroxymethyl-but-3-enyl)-cyclohexyl]-4-methyl-benzenesulfonamide (862115-11-5)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 34 percent / N-bromosuccinimide / 7 / 20 °C

2.1: BuLi; TMEDA / diethyl ether / 2 h / 0 - 20 °C

2.2: MgBr₂ / diethyl ether / 0 - 20 °C

2.3: 75 percent / diethyl ether / 2 h / 25 °C

With N-Bromosuccinimide; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; 7; In diethyl ether;

DOI:10.1021/ol050965t

upstream raw materials:

6-tert-butyl-1-(toluene-4-sulfonyl)-1-aza-spiro[2.5]octane

3-hydroxy-2-methyl-1-propene

1-tert-butyl-4-methylenecyclohexane

chloroamine-T