N-[2-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-benzenesulfonamide

Base Information

Chemical Name:N-[2-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-benzenesulfonamide
CAS No.:78073-17-3
Molecular Formula:C₁₈H₁₉NO₃S₂
Molecular Weight:361.486
Hs Code.:

Synonyms:N-[2-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-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-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-benzenesulfonamide

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Technology Process of N-[2-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-benzenesulfonamide

There total 3 articles about N-[2-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-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: 100.0%

: 54756-19-3
2,6-dimethyl-1-(p-tolylsulphonylimino)thiochroman-4-one

: 78073-17-3
N-[2-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-benzenesulfonamide

Guidance literature:: With triethylamine; In chloroform;
DOI:10.1039/P19810001037

Reference yield: 62.0%

: 35492-93-4
2,6-dimethyl-1-thiochroman-4-one

: 54756-19-3
2,6-dimethyl-1-(p-tolylsulphonylimino)thiochroman-4-one

: 78073-17-3
N-[2-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-benzenesulfonamide

: 78073-18-4
2,6-dimethyl-4-oxothiochroman S-oxide

Guidance literature:: With chloroamine-T; acetic acid; In methanol; at 0 ℃;
DOI:10.1039/P19810001037

Reference yield:

: 35492-93-4
2,6-dimethyl-1-thiochroman-4-one

: 78073-17-3
N-[2-((E)-But-2-enoyl)-4-methyl-phenylsulfanyl]-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / chloramine-T trihydrate, acetic acid / methanol / 0 °C

2: 100 percent / triethylamine / CHCl₃

With chloroamine-T; acetic acid; triethylamine; In methanol; chloroform;
DOI:10.1039/P19810001037