((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone

Base Information

Chemical Name:((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone
CAS No.:109384-77-2
Molecular Formula:C₁₆H₁₂Cl₂O₃S
Molecular Weight:355.241
Hs Code.:

Synonyms:((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone

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Chemical Property of ((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone

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Technology Process of ((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone

There total 4 articles about ((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone 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: 87.0%

: 5535-51-3
p-chlorophenyl vinyl sulfone

: 19158-57-7
(2-(4-chlorophenyl)-2-oxoethyl)dimethylsulfonium bromide

: 109384-77-2
((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone

Guidance literature:: With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; In dichloromethane; for 5h; Ambient temperature;
DOI:10.1055/s-1987-27854

Reference yield: 64.0%

: 325829-89-8
[4-(4-chloro-benzenesulfonyl)-4,5-dihydro-1H-pyrazol-3-yl]-(4-chloro-phenyl)-methanone

: 109384-77-2
((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone

Guidance literature:: In ethylene glycol; at 200 - 230 ℃;

Reference yield: 43.0%

: C₁₃H₁₂Cl₂O₃

: 14752-66-0
sodium p-chlorobenzenesulphinate

: 109384-77-2
((1S,2R)-2-(4-chlorophenylsulfonyl)cyclopropyl)(4-chlorophenyl)methanone

Guidance literature:: With caesium carbonate; In dimethyl sulfoxide; at 80 ℃; for 6h; diastereoselective reaction;
DOI:10.1016/j.tet.2016.04.062