C₃₃H₃₈N₂O₆

Base Information

Chemical Name:C₃₃H₃₈N₂O₆
CAS No.:244228-08-8
Molecular Formula:C₃₃H₃₈N₂O₆
Molecular Weight:558.675
Hs Code.:

C<sub>33</sub>H<sub>38</sub>N<sub>2</sub>O<sub>6</sub>

Synonyms:C₃₃H₃₈N₂O₆

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Chemical Property of C₃₃H₃₈N₂O₆

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Technology Process of C₃₃H₃₈N₂O₆

There total 7 articles about C₃₃H₃₈N₂O₆ 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: 80.0%

: 244227-93-8
C₃₄H₄₂N₂O₇

: 244228-08-8
C₃₃H₃₈N₂O₆

Guidance literature:: With periodic acid; In tetrahydrofuran; at 20 ℃; for 0.0833333h;

Reference yield:

: 126410-45-5
tert-butyl (S)-{3-[4-(benzyloxy)phenyl]-1-[methoxy(methyl)amino]-1-oxo-propan-2-yl}carbamate

: 244228-08-8
C₃₃H₃₈N₂O₆

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium aluminium tetrahydride / diethyl ether / 0.17 h / 0 °C

2.1: magnesium sulfate / dichloromethane / 1 h / 20 °C

3.1: dichloromethane / -78 - 20 °C / Inert atmosphere

3.2: Reflux

4.1: ethyl acetate; water / 1 h / 20 °C

5.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / water; tert-butyl alcohol / 24 h / 20 °C

6.1: periodic acid / tetrahydrofuran / 0.08 h / 20 °C

With osmium(VIII) oxide; lithium aluminium tetrahydride; magnesium sulfate; 4-methylmorpholine N-oxide; periodic acid; In tetrahydrofuran; diethyl ether; dichloromethane; water; ethyl acetate; tert-butyl alcohol;

Reference yield:

: 2130-96-3,54784-43-9
O-benzyl-N-tert-butoxycarbonyl-L-tyrosine

: 244228-08-8
C₃₃H₃₈N₂O₆

Guidance literature:: Multi-step reaction with 7 steps

1.1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / dichloromethane; N,N-dimethyl-formamide / 20 °C

2.1: lithium aluminium tetrahydride / diethyl ether / 0.17 h / 0 °C

3.1: magnesium sulfate / dichloromethane / 1 h / 20 °C

4.1: dichloromethane / -78 - 20 °C / Inert atmosphere

4.2: Reflux

5.1: ethyl acetate; water / 1 h / 20 °C

6.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / water; tert-butyl alcohol / 24 h / 20 °C

7.1: periodic acid / tetrahydrofuran / 0.08 h / 20 °C

With osmium(VIII) oxide; lithium aluminium tetrahydride; magnesium sulfate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; 4-methylmorpholine N-oxide; periodic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; tert-butyl alcohol;