2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ⁵-phosphanylidene)-acetamide

Base Information

• Chemical Name: 2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ⁵-phosphanylidene)-acetamide
• CAS No.: 151231-87-7
• Molecular Formula: C₃₅H₂₉FNOP
• Molecular Weight: 529.594

Synonyms:2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ⁵-phosphanylidene)-acetamide

Chemical Property of 2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ⁵-phosphanylidene)-acetamide

Chemical Property:

Purity/Quality:

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Technology Process of 2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ⁵-phosphanylidene)-acetamide

There total 3 articles about 2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ⁵-phosphanylidene)-acetamide 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: 84.0%

[(4-Fluoro-phenyl)-((E)-3-phenyl-allylcarbamoyl)-methyl]-triphenyl-phosphonium; chloride → 2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ5-phosphanylidene)-acetamide (151231-87-7)

Guidance literature:

With sodium carbonate; In water; for 24h; Ambient temperature;

DOI:10.1016/S0040-4020(01)81880-9

Reference yield:

(N-cinnamylimino)triphenylphosphorane (151231-67-3) → 2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ5-phosphanylidene)-acetamide (151231-87-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 68 percent / benzene / 4 h / Ambient temperature

2: 84 percent / Na₂CO₃ / H₂O / 24 h / Ambient temperature

With sodium carbonate; In water; benzene;

DOI:10.1016/S0040-4020(01)81880-9

Reference yield:

triphenylphosphine (603-35-0) → 2-(4-Fluoro-phenyl)-N-((E)-3-phenyl-allyl)-2-(triphenyl-λ5-phosphanylidene)-acetamide (151231-87-7)

Guidance literature:

Multi-step reaction with 3 steps

1: benzene / 1 h / 70 °C

2: 68 percent / benzene / 4 h / Ambient temperature

3: 84 percent / Na₂CO₃ / H₂O / 24 h / Ambient temperature

With sodium carbonate; In water; benzene;

DOI:10.1016/S0040-4020(01)81880-9

upstream raw materials:

(N-cinnamylimino)triphenylphosphorane

triphenylphosphine

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