{[1-(Benzenesulfonyl)-3,4-dimethylcyclohex-3-en-1-yl]methyl}benzene

Base Information

• Chemical Name: {[1-(Benzenesulfonyl)-3,4-dimethylcyclohex-3-en-1-yl]methyl}benzene
• CAS No.: 73301-21-0
• Molecular Formula: C21H24O2S
• Molecular Weight: 340.486
• DSSTox Substance ID: DTXSID20502697
• Mol file: 73301-21-0.mol

Synonyms:73301-21-0;DTXSID20502697;{[1-(Benzenesulfonyl)-3,4-dimethylcyclohex-3-en-1-yl]methyl}benzene;AKOS024322072;[[3,4-DIMETHYL-1-(PHENYLSULFONYL)-3-CYCLOHEXEN-1-YL]METHYL]BENZENE

Chemical Property of {[1-(Benzenesulfonyl)-3,4-dimethylcyclohex-3-en-1-yl]methyl}benzene

Chemical Property:

• XLogP3: 4.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 340.14970118
• Heavy Atom Count: 24
• Complexity: 557

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1=C(CC(CC1)(CC2=CC=CC=C2)S(=O)(=O)C3=CC=CC=C3)C

Technology Process of {[1-(Benzenesulfonyl)-3,4-dimethylcyclohex-3-en-1-yl]methyl}benzene

There total 4 articles about {[1-(Benzenesulfonyl)-3,4-dimethylcyclohex-3-en-1-yl]methyl}benzene 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: 89.0%

benzyl bromide (100-39-0) + 1-phenylsulfonyl-3,4-dimethylcyclohex-3-ene (73301-14-1) → 1,2-dimethyl-4-benzyl-4-(phenylsulfonyl)cyclohexene (73301-21-0)

Guidance literature:

In tetrahydrofuran;

DOI:10.1021/ja00522a075

Reference yield:

PVS (5535-48-8) → 1,2-dimethyl-4-benzyl-4-(phenylsulfonyl)cyclohexene (73301-21-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 94 percent / benzene / 32 h / 135 °C

2: 89 percent / tetrahydrofuran

In tetrahydrofuran; benzene;

DOI:10.1021/ja00522a075

Reference yield:

1-bromo-2-phenylthioethane (4837-01-8) → 1,2-dimethyl-4-benzyl-4-(phenylsulfonyl)cyclohexene (73301-21-0)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium ethoxide / ethanol / 8 h / Heating

2: 78 percent / 30percent H₂O₂ / acetic acid / 1.) 70 deg C, 2.) reflux, 20 min

3: 93.7 percent / hydroquinone / benzene / 22 h / 135 °C

4: 1.) n-BuLi / 1.) THF, hexane, -60 deg C, 10 min, 2.) 2 h, RT

With n-butyllithium; dihydrogen peroxide; sodium ethanolate; hydroquinone; In ethanol; acetic acid; benzene;

DOI:10.1021/jo00173a039

upstream raw materials:

benzyl bromide

1-phenylsulfonyl-3,4-dimethylcyclohex-3-ene

PVS

1-bromo-2-phenylthioethane

Downstream raw materials:

1,2-dimethyl-4-benzylcyclohexene