Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-

Base Information

• Chemical Name: Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-
• CAS No.: 25917-49-1
• Molecular Formula: C15H13ClO4S
• Molecular Weight: 324.785
• DSSTox Substance ID: DTXSID00441954
• Nikkaji Number: J1.002.660A
• Wikidata: Q82258976
• Mol file: 25917-49-1.mol

Synonyms:25917-49-1;Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-;SCHEMBL2542303;DTXSID00441954;4'-Chloro-alpha-tosyloxyacetophenone

Chemical Property of Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-

Chemical Property:

• XLogP3: 3.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 324.0223078
• Heavy Atom Count: 21
• Complexity: 441

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)S(=O)(=O)OCC(=O)C2=CC=C(C=C2)Cl

Technology Process of Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-

There total 12 articles about Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]- 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: 100.0%

para-chloroacetophenone (99-91-2) + toluene-4-sulfonic acid (104-15-4) → 1-(4-chlorophenyl)-2-(p-tolylsulfonyloxy)ethanone (25917-49-1)

Guidance literature:

With potassium peroxymonosulfate; 4-tolyl iodide; In water; acetonitrile; at 60 ℃; for 3h; Inert atmosphere;

DOI:10.1055/s-0029-1218370

Reference yield: 98.0%

1-(p-chlorophenyl)ethyl alcohol (3391-10-4) + Poly[4-hydroxy(tosyloxy)iodo]styrene → 1-(4-chlorophenyl)-2-(p-tolylsulfonyloxy)ethanone (25917-49-1)

Guidance literature:

In chloroform; Heating;

DOI:10.1021/jo010333u

Reference yield: 96.0%

1-(p-chlorophenyl)ethyl alcohol (3391-10-4) + toluene-4-sulfonic acid (104-15-4) → 1-(4-chlorophenyl)-2-(p-tolylsulfonyloxy)ethanone (25917-49-1)

Guidance literature:

With iodosylbenzene; In acetonitrile; for 1.5h; Heating;

DOI:10.1021/jo030045t

upstream raw materials:

[hydroxy(tosyloxy)iodo]benzene

para-chloroacetophenone

silver(I) 4-methylbenzenesulfonate

4-chlorobenzoylmethyl bromide

Downstream raw materials:

3-(4-Chloro-phenyl)-5,6-dihydro-imidazo[2,1-b]thiazole; compound with toluene-4-sulfonic acid

1-(4-chloro-phenyl)-2-thiocyanato-ethanone

1-(4-chloro-phenyl)-2-p-toluidino-ethanone

1-(4-chlorophenyl)-2-(4-methoxyphenylamino)ethanone

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