(E)-N-(cyclohex-2-en-1-yl)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide

Base Information

• Chemical Name: (E)-N-(cyclohex-2-en-1-yl)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide
• CAS No.: 1647100-72-8
• Molecular Formula: C₁₈H₂₃NO₂S
• Molecular Weight: 317.452
• Mol file: 1647100-72-8.mol

Synonyms:(E)-N-(cyclohex-2-en-1-yl)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide

Chemical Property of (E)-N-(cyclohex-2-en-1-yl)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (E)-N-(cyclohex-2-en-1-yl)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide

There total 1 articles about (E)-N-(cyclohex-2-en-1-yl)-4-methyl-N-(penta-2,4-dien-1-yl)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%

(E)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide (136573-40-5) + Cyclohex-2-enol (822-67-3) → (E)-N-(cyclohex-2-en-1-yl)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide (1647100-72-8)

Guidance literature:

With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃; for 48h; Inert atmosphere;

DOI:10.1002/anie.201405359

Reference yield:

(E)-N-(cyclohex-2-en-1-yl)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide (1647100-72-8) → 1-tosyl-3-vinyldecahydrocyclobuta[cd]indole + 1-tosyl-3-vinyldecahydrocyclobuta[cd]indole

Guidance literature:

With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; In dimethyl sulfoxide; at 20 ℃; for 18h; Concentration; Overall yield = 94 %; Overall yield = 94 mg; Schlenk technique; Irradiation;

DOI:10.1002/anie.201405359

upstream raw materials:

(E)-4-methyl-N-(penta-2,4-dien-1-yl)benzenesulfonamide

Cyclohex-2-enol