C₂₇H₃₀N₂O

Base Information

Chemical Name:C₂₇H₃₀N₂O
CAS No.:912338-18-2
Molecular Formula:C₂₇H₃₀N₂O
Molecular Weight:398.548
Hs Code.:

C<sub>27</sub>H<sub>30</sub>N<sub>2</sub>O

Synonyms:C₂₇H₃₀N₂O

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₇H₃₀N₂O

Chemical Property:

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Technology Process of C₂₇H₃₀N₂O

There total 4 articles about C₂₇H₃₀N₂O 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:

: 867324-06-9
N-phenethylbut-3-en-1-amine

: C₁₅H₁₄NO₂^(1-)*K⁽¹⁺⁾

: 912338-18-2
C₂₇H₃₀N₂O

Guidance literature:: With pivaloyl chloride; In dichloromethane; at 0 - 20 ℃; for 17h;

Reference yield:

: 3886-70-2
(R)-1-(1-Naphthyl)ethylamine

: 912338-18-2
C₂₇H₃₀N₂O

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / acetonitrile / 18 h / 20 - 60 °C / Inert atmosphere; Large scale

2.1: potassium trimethylsilonate / tetrahydrofuran / 16.33 h / 20 - 30 °C / Inert atmosphere; Large scale

2.2: 1 h / 0 - 20 °C / Inert atmosphere; Large scale

3.1: tetrahydrofuran; dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere; Large scale

With potassium trimethylsilonate; potassium carbonate; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/op700073g

Reference yield:

: 64-04-0
phenethylamine

: 912338-18-2
C₂₇H₃₀N₂O

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 15.5 h / 20 - 50 °C / Inert atmosphere

2: tetrahydrofuran; dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere; Large scale

With potassium carbonate; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/op700073g