C₂₈H₃₄N₂O₃

Base Information

Chemical Name:C₂₈H₃₄N₂O₃
CAS No.:898254-23-4
Molecular Formula:C₂₈H₃₄N₂O₃
Molecular Weight:446.59
Hs Code.:

C<sub>28</sub>H<sub>34</sub>N<sub>2</sub>O<sub>3</sub>

Synonyms:C₂₈H₃₄N₂O₃

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Chemical Property of C₂₈H₃₄N₂O₃

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Technology Process of C₂₈H₃₄N₂O₃

There total 6 articles about C₂₈H₃₄N₂O₃ 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:

: 13335-71-2
2-(2,6-dimethylphenoxy)acetic acid

: 898254-23-4
C₂₈H₃₄N₂O₃

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / DMF / ethyl acetate / 6 h / 20 - 50 °C

2: aq. NaHCO₃ / ethyl acetate / 1 h / 20 °C

3: HCO₂NH₄ / Pd/C / methanol / 50 °C

With thionyl chloride; ammonium formate; sodium hydrogencarbonate; palladium on activated charcoal; N,N-dimethyl-formamide; In methanol; ethyl acetate;
DOI:10.1021/jm070284z

Reference yield:

: 20143-48-0
2,6-dimethylphenoxyacetyl chloride

: 898254-23-4
C₂₈H₃₄N₂O₃

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaHCO₃ / ethyl acetate / 1 h / 20 °C

2: HCO₂NH₄ / Pd/C / methanol / 50 °C

With ammonium formate; sodium hydrogencarbonate; palladium on activated charcoal; In methanol; ethyl acetate;
DOI:10.1021/jm070284z

Reference yield:

: 156732-13-7
(S,E)-5-amino-2-(dibenzylamino)-1,6-diphenylhex-4-en-3-one

: 898254-23-4
C₂₈H₃₄N₂O₃

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium tetrahydroborate; methanesulfonic acid / diethylene glycol dimethyl ether; isopropyl alcohol / 12 h / 0 - 5 °C

1.2: 0.5 h / 0 - 5 °C

1.3: 3 h / 15 °C

2.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 4 h / 20 °C

3.1: ammonium formate; palladium 10% on activated carbon / methanol / 15 h / 50 °C

With sodium tetrahydroborate; methanesulfonic acid; palladium 10% on activated carbon; ammonium formate; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In methanol; diethylene glycol dimethyl ether; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1021/acs.jmedchem.0c00529