C₃₂H₄₀IN₃O₃

Base Information

Chemical Name:C₃₂H₄₀IN₃O₃
CAS No.:1361944-81-1
Molecular Formula:C₃₂H₄₀IN₃O₃
Molecular Weight:641.592
Hs Code.:

C<sub>32</sub>H<sub>40</sub>IN<sub>3</sub>O<sub>3</sub>

Synonyms:

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Chemical Property of C₃₂H₄₀IN₃O₃

Chemical Property:

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Technology Process of C₃₂H₄₀IN₃O₃

There total 9 articles about C₃₂H₄₀IN₃O₃ 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:

: C₁₈H₂₉NO₃Si

: 1361944-81-1
C₃₂H₄₀IN₃O₃

Guidance literature:: Multi-step reaction with 6 steps

1: N-Bromosuccinimide / tetrahydrofuran / -40 °C

2: sodium tetrahydroborate / ethanol / -78 °C

3: potassium hydroxide / ethanol

4: isopropyl alcohol / 70 °C

5: dichloromethane / 0 °C

6: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / 0 - 20 °C

With sodium tetrahydroborate; N-Bromosuccinimide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; isopropyl alcohol;
DOI:10.1002/chem.201102078

Reference yield:

: 388073-12-9
C₂₂H₂₉IN₂O₃

: 1361944-81-1
C₃₂H₄₀IN₃O₃

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 0 °C

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / 0 - 20 °C

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane;
DOI:10.1002/chem.201102078

Reference yield:

: 85613-64-5
(S)-3-(tert-butoxycarbonyl)amino-4-phenyl-2-butanone

: 1361944-81-1
C₃₂H₄₀IN₃O₃

Guidance literature:: Multi-step reaction with 7 steps

1: lithium hexamethyldisilazane / tetrahydrofuran

2: N-Bromosuccinimide / tetrahydrofuran / -40 °C

3: sodium tetrahydroborate / ethanol / -78 °C

4: potassium hydroxide / ethanol

5: isopropyl alcohol / 70 °C

6: dichloromethane / 0 °C

7: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / 0 - 20 °C

With sodium tetrahydroborate; N-Bromosuccinimide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; potassium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol; dichloromethane; isopropyl alcohol;
DOI:10.1002/chem.201102078