[(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide

Base Information

Chemical Name:[(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide
CAS No.:1367876-30-9
Molecular Formula:Br*C₂₉H₂₅NO₄P
Molecular Weight:562.4
Hs Code.:

Synonyms:[(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide

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Chemical Property of [(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide

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Technology Process of [(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide

There total 3 articles about [(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide 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: 95.0%

: 1026256-04-1
C₁₁H₁₀BrNO₄

: 603-35-0
triphenylphosphine

: 1367876-30-9
[(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide

Guidance literature:: In acetonitrile; at 25 ℃; for 24h;
DOI:10.1002/hc.21001

Reference yield:

: 360574-95-4
2-[hydroxy-(3-nitro-phenyl)-methyl]-acrylic acid methyl ester

: 1367876-30-9
[(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide

Guidance literature:: Multi-step reaction with 2 steps

1: lithium bromide / Acidic conditions

2: acetonitrile / 24 h / 25 °C

With lithium bromide; In acetonitrile;
DOI:10.1002/hc.21001

Reference yield:

: 99-61-6
3-nitro-benzaldehyde

: 1367876-30-9
[(Z)-2-methoxycarbonyl-3-(3-nitrophenyl)-2-propenyl]triphenylphosphonium bromide

Guidance literature:: Multi-step reaction with 3 steps

2: lithium bromide / Acidic conditions

3: acetonitrile / 24 h / 25 °C

With lithium bromide; In acetonitrile; 1: Morita-Baylis-Hillman reaction;
DOI:10.1002/hc.21001