C₂₉H₃₆N₂O₅

Base Information

Chemical Name:C₂₉H₃₆N₂O₅
CAS No.:1092938-21-0
Molecular Formula:C₂₉H₃₆N₂O₅
Molecular Weight:492.615
Hs Code.:

C<sub>29</sub>H<sub>36</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:C₂₉H₃₆N₂O₅

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Chemical Property of C₂₉H₃₆N₂O₅

Chemical Property:

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Technology Process of C₂₉H₃₆N₂O₅

There total 10 articles about C₂₉H₃₆N₂O₅ 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: 64.0%

: 850036-28-1
cyclopenten-1-ylboronic acid

: 1092938-86-7
tert-butyl (6R)-6-{[6-bromo-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}heptanoate

: 1092938-21-0
C₂₉H₃₆N₂O₅

Guidance literature:: With sodium carbonate; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; water; for 1.5h; Reflux; Inert atmosphere;

Reference yield:

: 62327-21-3
tert-butyl dimethylphosphonoacetate

: 1092938-21-0
C₂₉H₃₆N₂O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / tetrahydrofuran / 0.5 h / 20 °C / Cooling

1.2: -78 - 20 °C

2.1: hydrogen / palladium 10% on activated carbon / ethanol / 2 h / 20 °C / 760.05 Torr

3.1: phosphazene base-P₄-tert-butyl / hexane; tetrahydrofuran / 2.66 h / -10 - 20 °C / Inert atmosphere

4.1: N-Bromosuccinimide / acetonitrile / 2 h / 20 °C / Inert atmosphere

5.1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / water; tetrahydrofuran / 1.5 h / Reflux; Inert atmosphere

With N-Bromosuccinimide; hydrogen; sodium hydride; sodium carbonate; phosphazene base-P₄-tert-butyl; bis-triphenylphosphine-palladium(II) chloride; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; hexane; water; acetonitrile;

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 1092938-21-0
C₂₉H₃₆N₂O₅

Guidance literature:: Multi-step reaction with 6 steps

1.1: N,N-dimethylammonium chloride; potassium fluoride / dichloromethane; xylene / 15 h / 160 °C

2.1: ethanol / 0.17 h / 85 °C

2.2: 15 h / 85 °C

3.1: N,N-diethylaniline; trichlorophosphate / toluene / 37 h / 100 °C

4.1: phosphazene base-P₄-tert-butyl / hexane; tetrahydrofuran / 2.66 h / -10 - 20 °C / Inert atmosphere

5.1: N-Bromosuccinimide / acetonitrile / 2 h / 20 °C / Inert atmosphere

6.1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / water; tetrahydrofuran / 1.5 h / Reflux; Inert atmosphere

With potassium fluoride; N-Bromosuccinimide; N,N-dimethylammonium chloride; sodium carbonate; phosphazene base-P₄-tert-butyl; N,N-diethylaniline; trichlorophosphate; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; ethanol; hexane; dichloromethane; water; toluene; acetonitrile; xylene;