C₁₉H₃₀N₂O₃

Base Information

Chemical Name:C₁₉H₃₀N₂O₃
CAS No.:1220904-25-5
Molecular Formula:C₁₉H₃₀N₂O₃
Molecular Weight:334.459
Hs Code.:

C<sub>19</sub>H<sub>30</sub>N<sub>2</sub>O<sub>3</sub>

Synonyms:C₁₉H₃₀N₂O₃

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Chemical Property of C₁₉H₃₀N₂O₃

Chemical Property:

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Technology Process of C₁₉H₃₀N₂O₃

There total 6 articles about C₁₉H₃₀N₂O₃ 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: 97.0%

: 1220904-24-4
C₂₄H₃₈N₂O₅

: 1220904-25-5
C₁₉H₃₀N₂O₃

Guidance literature:: C₂₄H₃₈N₂O₅; With trifluoroacetic acid; In dichloromethane; for 2h;

With sodium hydroxide; In dichloromethane; water;

Reference yield:

: 70240-29-8
4-(isopropyloxycarbonyl)benzaldehyde

: 1220904-25-5
C₁₉H₃₀N₂O₃

Guidance literature:: Multi-step reaction with 5 steps

1.1: caesium carbonate / dichloromethane / 30 h / 42 °C

2.1: magnesium / iodine / diethyl ether / 2.75 h / Inert atmosphere; Reflux

2.2: 2 h / -78 - 20 °C

2.3: 1 h / 0 - 20 °C

3.1: hydrogenchloride / 1,4-dioxane; methanol / 1.5 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / acetonitrile / 16.25 h / 0 - 20 °C

5.1: trifluoroacetic acid / dichloromethane / 2 h

With hydrogenchloride; benzotriazol-1-ol; caesium carbonate; magnesium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; iodine; In 1,4-dioxane; methanol; diethyl ether; dichloromethane; acetonitrile;

Reference yield:

: 1220904-43-7
(S)-isopropyl 4-((tert-butylsulfinylimino)methyl)benzoate

: 1220904-25-5
C₁₉H₃₀N₂O₃

Guidance literature:: Multi-step reaction with 4 steps

1.1: magnesium / iodine / diethyl ether / 2.75 h / Inert atmosphere; Reflux

1.2: 2 h / -78 - 20 °C

1.3: 1 h / 0 - 20 °C

2.1: hydrogenchloride / 1,4-dioxane; methanol / 1.5 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / acetonitrile / 16.25 h / 0 - 20 °C

4.1: trifluoroacetic acid / dichloromethane / 2 h

With hydrogenchloride; benzotriazol-1-ol; magnesium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; iodine; In 1,4-dioxane; methanol; diethyl ether; dichloromethane; acetonitrile;