2-[(Phenylsulfonyl)methyl]pyridine

Base Information

• Chemical Name: 2-[(Phenylsulfonyl)methyl]pyridine
• CAS No.: 1620-50-4
• Molecular Formula: C12H11NO2S
• Molecular Weight: 233.291
• European Community (EC) Number: 665-091-7
• Nikkaji Number: J2.091.812H
• Mol file: 1620-50-4.mol

Synonyms:2-[(phenylsulfonyl)methyl]pyridine;2-[(benzenesulfonyl)methyl]pyridine;1620-50-4;phenyl 2-picolyl sulfone;2-benzenesulfonylmethyl-pyridine;2-Benzenesulphonylmethylpyridine;SCHEMBL2070900;Phenyl(2-pyridylmethyl) sulfone;PPFKQEVWJGRSJC-UHFFFAOYSA-N;2-(benzenesulfonyl-methyl)-pyridine;AKOS024324087

Chemical Property of 2-[(Phenylsulfonyl)methyl]pyridine

Chemical Property:

• XLogP3: 1.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 233.05104977
• Heavy Atom Count: 16
• Complexity: 302

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)S(=O)(=O)CC2=CC=CC=N2

Technology Process of 2-[(Phenylsulfonyl)methyl]pyridine

There total 13 articles about 2-[(Phenylsulfonyl)methyl]pyridine 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: 98.0%

sodium benzenesulfonate (873-55-2) + 2-chloromethylpyridine hydrochloride (6959-47-3) → 2-<(phenylsulfonyl)methyl>pyridine (1620-50-4)

Guidance literature:

With tetra-n-propylammonium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 80 ℃; for 24h;

DOI:10.1055/s-2004-822311

Reference yield: 80.0%

sodium benzenesulfonate (873-55-2) + 2-(bromomethyl)pyridine hydrobromide (31106-82-8) → 2-<(phenylsulfonyl)methyl>pyridine (1620-50-4)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 48h;

Reference yield: 76.0%

2-[(phenylsulfanyl)methyl]pyridine (71897-63-7) → 2-<(phenylsulfonyl)methyl>pyridine (1620-50-4)

Guidance literature:

With tetra-n-butylammonium peroxomonosulfate; In dichloromethane; for 24h; Ambient temperature;

DOI:10.1021/jo00238a011

upstream raw materials:

2-chloromethylpyridine

sodium benzenesulfonate

2-[(phenylsulfanyl)methyl]pyridine

2-chloromethylpyridine hydrochloride

Downstream raw materials:

2-(benzenesulfonylmethyl)pyridine N-oxide

benzyl dithiopicolinate

2-(2-phenylethynyl)pyridine

4-[(pyridine-2-carbothioylsulfanyl)methyl]benzoic acid

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