C₃₂H₃₆N₂O₃

Base Information

Chemical Name:C₃₂H₃₆N₂O₃
CAS No.:312754-19-1
Molecular Formula:C₃₂H₃₆N₂O₃
Molecular Weight:496.649
Hs Code.:

C<sub>32</sub>H<sub>36</sub>N<sub>2</sub>O<sub>3</sub>

Synonyms:

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Chemical Property of C₃₂H₃₆N₂O₃

Chemical Property:

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Technology Process of C₃₂H₃₆N₂O₃

There total 10 articles about C₃₂H₃₆N₂O₃ 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: 30.0%

: 173140-90-4
(R)-5-(2-oxiranyl)-8-benzyloxy-2(1H)-quinolinone

: 312754-11-3
5,6-diethyl-2-methyl-indan-2-ylamine

: 312754-19-1
C₃₂H₃₆N₂O₃

Guidance literature:: In butan-1-ol; at 100 ℃; for 1.25h; Microwave irradiation;
DOI:10.1016/j.bmcl.2012.07.096

Reference yield:

: 17496-14-9
2,3-dihydro-2-methyl-1H-inden-1-one

: 312754-19-1
C₃₂H₃₆N₂O₃

Guidance literature:: Multi-step reaction with 12 steps

1: potassium hexacyanoferrate(III); ammonia / water / 10 h / 80 °C / Inert atmosphere

2: tetrahydrofuran / 18 h / 25 °C

3: hydrogen; 10% Pd/C; sulfuric acid; acetic acid / 18 h / 25 °C / 760.05 Torr

4: sodium hydroxide / water / 1 h / 25 °C

5: triethylamine / dichloromethane / 1 h / 25 °C

6: aluminum (III) chloride / nitromethane / 4 h / 25 °C

7: hydrogen; 10% Pd/C / ethanol / 48 h / 25 °C / 760.05 Torr

8: aluminum (III) chloride / nitromethane / 3 h / 25 °C

9: hydrogen; 10% Pd/C / ethanol / 24 h / 25 °C / 760.05 Torr

10: lithium aluminium tetrahydride / tetrahydrofuran / 72 h / Reflux

11: hydrogen; 10% Pd/C / ethanol / 18 h / 25 °C / 760.05 Torr

12: butan-1-ol / 1.25 h / 100 °C / Microwave irradiation

With aluminum (III) chloride; lithium aluminium tetrahydride; sulfuric acid; 10% Pd/C; ammonia; hydrogen; acetic acid; triethylamine; sodium hydroxide; potassium hexacyanoferrate(III); In tetrahydrofuran; nitromethane; ethanol; dichloromethane; water; butan-1-ol; 6: |Friedel-Crafts Acylation / 8: |Friedel-Crafts Acylation;
DOI:10.1016/j.bmcl.2012.07.096

Reference yield:

: 312754-06-6
N-(5-acetyl-2-methyl-indan-2-yl)-benzamide

: 312754-19-1
C₃₂H₃₆N₂O₃

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogen; 10% Pd/C / ethanol / 48 h / 25 °C / 760.05 Torr

2: aluminum (III) chloride / nitromethane / 3 h / 25 °C

3: hydrogen; 10% Pd/C / ethanol / 24 h / 25 °C / 760.05 Torr

4: lithium aluminium tetrahydride / tetrahydrofuran / 72 h / Reflux

5: hydrogen; 10% Pd/C / ethanol / 18 h / 25 °C / 760.05 Torr

6: butan-1-ol / 1.25 h / 100 °C / Microwave irradiation

With aluminum (III) chloride; lithium aluminium tetrahydride; 10% Pd/C; hydrogen; In tetrahydrofuran; nitromethane; ethanol; butan-1-ol; 2: |Friedel-Crafts Acylation;
DOI:10.1016/j.bmcl.2012.07.096