C₃₄H₄₆N₄O₅

Base Information

Chemical Name:C₃₄H₄₆N₄O₅
CAS No.:1613625-06-1
Molecular Formula:C₃₄H₄₆N₄O₅
Molecular Weight:590.763
Hs Code.:

C<sub>34</sub>H<sub>46</sub>N<sub>4</sub>O<sub>5</sub>

Synonyms:C₃₄H₄₆N₄O₅

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Chemical Property of C₃₄H₄₆N₄O₅

Chemical Property:

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Technology Process of C₃₄H₄₆N₄O₅

There total 17 articles about C₃₄H₄₆N₄O₅ 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:

: 58885-58-8
N-tert-butoxycarbonyl-3-aminopropanol

: 1613625-06-1
C₃₄H₄₆N₄O₅

Guidance literature:: Multi-step reaction with 2 steps

1: Dess-Martin periodane / dichloromethane / 2 h / 0 - 20 °C

2: acetic acid; sodium cyanoborohydride / methanol / 19 h / 20 °C

With sodium cyanoborohydride; Dess-Martin periodane; acetic acid; In methanol; dichloromethane;

Reference yield:

: 58885-60-2
N-(tert-butoxycarbonyl)-3-aminopropanal

: 1613625-05-0
C₂₆H₃₁N₃O₃

: 1613625-06-1
C₃₄H₄₆N₄O₅

Guidance literature:: With sodium cyanoborohydride; acetic acid; In methanol; at 20 ℃; for 19h;

Reference yield:

: 10465-20-0
γ-(4-methoxy-1-naphthyl)butyric acid

: 1613625-06-1
C₃₄H₄₆N₄O₅

Guidance literature:: Multi-step reaction with 16 steps

1.1: n-butyllithium / tetrahydrofuran / 0.75 h / -78 °C

1.2: 3.5 h / 0 - 20 °C

2.1: potassium hexamethylsilazane / tetrahydrofuran / 0.5 h / -78 °C

2.2: -78 °C

2.3: 16 h / -78 - 27 °C

3.1: dihydrogen peroxide; lithium hydroxide / tetrahydrofuran; water / 3 h / 0 °C

4.1: hydrogen; palladium 10% on activated carbon / water / 3 h / 20 °C / 760.05 Torr

5.1: acetic acid; hydrogen bromide / 4 h / Reflux

6.1: acetyl chloride / 4 h / 0 °C / Reflux

7.1: sodium hydrogencarbonate / methanol; water / 3 h / 0 - 20 °C

8.1: pyridine / 2.5 h / 0 - 20 °C

9.1: tri-tert-butyl phosphine; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine / acetonitrile; hexane / 5 h / Inert atmosphere; Reflux

10.1: sodium hydroxide; water / tetrahydrofuran; methanol / 3 h / 20 °C

11.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.5 h / 0 °C

12.1: ammonia / methanol / 18 h / 0 - 20 °C

13.1: hydrogen; palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 760.05 Torr

14.1: triethylamine / dichloromethane / 2 h / 0 - 20 °C

15.1: hydrogenchloride / tetrahydrofuran; 1,4-dioxane / 6 h / 20 °C

16.1: acetic acid; sodium cyanoborohydride / methanol / 19 h / 20 °C

With 4-methyl-morpholine; pyridine; hydrogenchloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; tri-tert-butyl phosphine; palladium 10% on activated carbon; ammonia; water; hydrogen bromide; hydrogen; dihydrogen peroxide; potassium hexamethylsilazane; sodium cyanoborohydride; sodium hydrogencarbonate; acetic acid; triethylamine; acetyl chloride; sodium hydroxide; lithium hydroxide; isobutyl chloroformate; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; hexane; dichloromethane; water; acetonitrile;