2-benzenesulfinylpropionaldehyde

Base Information

Chemical Name:2-benzenesulfinylpropionaldehyde
CAS No.:84018-76-8
Molecular Formula:C₉H₁₀O₂S
Molecular Weight:182.243
Hs Code.:

Synonyms:2-benzenesulfinylpropionaldehyde

Suppliers and Price of 2-benzenesulfinylpropionaldehyde

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-benzenesulfinylpropionaldehyde

Chemical Property:

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Technology Process of 2-benzenesulfinylpropionaldehyde

There total 3 articles about 2-benzenesulfinylpropionaldehyde 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:

: 201230-82-2
carbon monoxide

: 20451-53-0
Phenyl vinyl sulfoxide

: 84018-76-8
2-benzenesulfinylpropionaldehyde

Guidance literature:: With hydrogen; (1,5-COD)RhBPh₄; 1,4-di(diphenylphosphino)-butane; In dichloromethane; at 75 ℃; for 2h; under 31028.9 Torr; Product distribution; Mechanism; time course of the reaction; also at r. t; use of other catalysts to achieve diastereo-and enantioselectivity; sulfones as further substrates;
DOI:10.1021/jo00064a019

Reference yield:

: 55064-96-5
2-(phenylthio)propanal

: 84018-76-8
2-benzenesulfinylpropionaldehyde

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 0.416667h;
DOI:10.1248/cpb.30.3054

Reference yield:

: 69994-64-5
2-benzenesulfenylpropionaldehyde diethylacetal

: 84018-76-8
2-benzenesulfinylpropionaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: cc HCl / acetonitrile / 0.33 h

2: m-CPBA / CH₂Cl₂ / 0.42 h

With hydrogenchloride; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetonitrile;
DOI:10.1248/cpb.30.3054