C₂₅H₃₄N₂O₅

Base Information

Chemical Name:C₂₅H₃₄N₂O₅
CAS No.:1354967-43-3
Molecular Formula:C₂₅H₃₄N₂O₅
Molecular Weight:442.555
Hs Code.:

C<sub>25</sub>H<sub>34</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:

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Chemical Property of C₂₅H₃₄N₂O₅

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Technology Process of C₂₅H₃₄N₂O₅

There total 3 articles about C₂₅H₃₄N₂O₅ 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:

: 4-(2-[cyclopentyloxy]ethoxy)phenol

: 1354967-43-3
C₂₅H₃₄N₂O₅

Guidance literature:: Multi-step reaction with 4 steps

1.1: N,N-dimethyl-formamide; mineral oil / 0.33 h / 20 °C / Inert atmosphere

1.2: 7 h

2.1: ethanol / 0.5 h / 100 °C / 12929 Torr / MW reactor

3.1: hydrogen; acetic acid / palladium 10% on activated carbon / water; methanol / 5 h / 2585.81 Torr

3.2: 1 h / 20 °C

4.1: triethylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / dichloromethane / 20 °C

With hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; triethylamine; palladium 10% on activated carbon; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 86596-60-3
2-{4-[2-(cyclopentyloxy)ethoxy]phenoxymethyl}oxirane

: 1354967-43-3
C₂₅H₃₄N₂O₅

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanol / 0.5 h / 100 °C / 12929 Torr / MW reactor

2.1: hydrogen; acetic acid / palladium 10% on activated carbon / water; methanol / 5 h / 2585.81 Torr

2.2: 1 h / 20 °C

3.1: triethylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / dichloromethane / 20 °C

With hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; triethylamine; palladium 10% on activated carbon; In methanol; ethanol; dichloromethane; water;

Reference yield:

: 1354968-49-2
tert-butyl 2-(benzyl(3-(4-(2-(cyclopentyloxy)ethoxy)phenoxy)-2-hydroxypropyl)amino)ethylcarbamate

: 1354967-43-3
C₂₅H₃₄N₂O₅

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen; acetic acid / palladium 10% on activated carbon / water; methanol / 5 h / 2585.81 Torr

1.2: 1 h / 20 °C

2.1: triethylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / dichloromethane / 20 °C

With hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; triethylamine; palladium 10% on activated carbon; In methanol; dichloromethane; water;