N-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]benzenesulfonamide

Base Information

Chemical Name:N-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]benzenesulfonamide
CAS No.:1342341-27-8
Molecular Formula:C₂₅H₃₂BrNO₂SSi
Molecular Weight:518.59
Hs Code.:

Synonyms:N-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]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-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]benzenesulfonamide

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Technology Process of N-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]benzenesulfonamide

There total 6 articles about N-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]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%

: 1342341-26-7
4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]benzenesulfonamide

: 2048-31-9,66820-54-0
(Z)-2-bromo-3-phenylprop-2-en-1-ol

: 1342341-27-8
N-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]benzenesulfonamide

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1055/s-0030-1260098

Reference yield:

: C₂₁H₃₃NO₄SSi

: 1342341-27-8
N-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride; water / ethyl acetate / 4 h / 50 °C

2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0 - 20 °C

With hydrogenchloride; di-isopropyl azodicarboxylate; water; triphenylphosphine; In tetrahydrofuran; ethyl acetate;
DOI:10.1055/s-0030-1260098

Reference yield:

: 21788-36-3
(Z)-methyl 2-bromo-3-phenylacrylate

: 1342341-27-8
N-[(Z)-2-bromo-3-phenylprop-2-enyl]-4-methyl-N-[(1R)-4-methyl-1-(trimethylsilyl)pent-1-yn-3-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: diisobutylaluminium hydride / tetrahydrofuran

2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0 - 20 °C

With di-isopropyl azodicarboxylate; diisobutylaluminium hydride; triphenylphosphine; In tetrahydrofuran;
DOI:10.1055/s-0030-1260098