N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide

Base Information

Chemical Name:N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide
CAS No.:779357-92-5
Molecular Formula:C₃₀H₃₄NO₄PS
Molecular Weight:535.644
Hs Code.:

<i>N</i>-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-<i>N</i>-oxiranylmethyl-benzenesulfonamide

Synonyms:N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide

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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 N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide

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Technology Process of N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide

There total 4 articles about N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide 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: 75.0%

: 5997-56-8
4-methyl-N-(oxiran-2-ylmethyl)benzenesulfonamide

: 779358-13-3
C₂₀H₂₂BrOP

: 779357-92-5
N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide

Guidance literature:: With potassium carbonate; In acetone; at 40 ℃;
DOI:10.1002/anie.200460099 DOI:10.1055/s-2005-865357

Reference yield:

: 862012-85-9
1-[1-(diphenyl-phosphinoyl)-vinyl]-cyclohexanol

: 779357-92-5
N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 40 percent / NBS; Me₂S / CH₂Cl₂ / 20 °C

2: 75 percent / K₂CO₃ / acetone / 40 °C

With N-Bromosuccinimide; dimethylsulfide; potassium carbonate; In dichloromethane; acetone;
DOI:10.1055/s-2005-865357

Reference yield:

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 779357-92-5
N-[2-cyclohexylidene-2-(diphenyl-phosphinoyl)-ethyl]-4-methyl-N-oxiranylmethyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 40 percent / LDA / -78 °C

2: 40 percent / NBS; Me₂S / CH₂Cl₂ / 20 °C

3: 75 percent / K₂CO₃ / acetone / 40 °C

With N-Bromosuccinimide; dimethylsulfide; potassium carbonate; lithium diisopropyl amide; In dichloromethane; acetone;
DOI:10.1055/s-2005-865357