C₂₇H₃₅N₃O

Base Information

Chemical Name:C₂₇H₃₅N₃O
CAS No.:1334476-40-2
Molecular Formula:C₂₇H₃₅N₃O
Molecular Weight:417.594
Hs Code.:

C<sub>27</sub>H<sub>35</sub>N<sub>3</sub>O

Synonyms:C₂₇H₃₅N₃O

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Chemical Property of C₂₇H₃₅N₃O

Chemical Property:

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Technology Process of C₂₇H₃₅N₃O

There total 7 articles about C₂₇H₃₅N₃O 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: 56.0%

: 39742-60-4
1-(2-phenylethyl)-4-piperidinone

: 362603-40-5
1-methyl-2-(3,7,8,9-tetrahydro-pyrano[3,2-e]indol-1-yl)-ethylamine

: 1334476-40-2
C₂₇H₃₅N₃O

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 18h; under 2280.15 Torr;
DOI:10.1016/j.tetlet.2011.07.058

Reference yield:

: 1334476-35-5
C₁₄H₁₄N₂O₃

: 1334476-40-2
C₂₇H₃₅N₃O

Guidance literature:: Multi-step reaction with 3 steps

1: bromobenzene / Reflux

2: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C / 2280.15 Torr

3: palladium 10% on activated carbon; hydrogen / ethanol / 18 h / 20 °C / 2280.15 Torr

With palladium 10% on activated carbon; hydrogen; In bromobenzene; ethanol; 1: Claisen rearrangement;
DOI:10.1016/j.tetlet.2011.07.058

Reference yield:

: C₁₄H₁₄N₂O₃

: 1334476-40-2
C₂₇H₃₅N₃O

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C / 2280.15 Torr

2: palladium 10% on activated carbon; hydrogen / ethanol / 18 h / 20 °C / 2280.15 Torr

With palladium 10% on activated carbon; hydrogen; In ethanol;
DOI:10.1016/j.tetlet.2011.07.058