C₁₉H₂₀FNO

Base Information

Chemical Name:C₁₉H₂₀FNO
CAS No.:561280-12-4
Molecular Formula:C₁₉H₂₀FNO
Molecular Weight:297.372
Hs Code.:

Synonyms:

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Chemical Property of C₁₉H₂₀FNO

Chemical Property:

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Technology Process of C₁₉H₂₀FNO

There total 6 articles about C₁₉H₂₀FNO 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:

: 561280-07-7
(1R,8S,9S)-(+)-5-(2-fluorophenyl)-8,10,10-trimethyl-6-azatricyclo[7.1.1.0^2,7]undeca-2⁽⁷⁾,3,5-triene

: 561280-12-4
C₁₉H₂₀FNO

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 - 20 ℃; for 2h; Inert atmosphere;
DOI:10.1002/chem.201203817

Reference yield:

: 7785-26-4,25766-18-1
(-)-α-pinene

: 561280-12-4
C₁₉H₂₀FNO

Guidance literature:: Multi-step reaction with 4 steps

1.1: 5,15,10,20-tetraphenylporphyrin; acetic anhydride / Inert atmosphere

2.1: ammonium acetate / acetic acid / 110 °C / Inert atmosphere

2.2: 48 h / 110 °C / Inert atmosphere

3.1: n-butyllithium; diisopropylamine / hexane; tetrahydrofuran / 2 h / -40 °C / Inert atmosphere

3.2: 20 °C / Inert atmosphere

4.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

With n-butyllithium; ammonium acetate; 5,15,10,20-tetraphenylporphyrin; acetic anhydride; diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; hexane; dichloromethane; acetic acid; 2.1: |Kroehnke Pyridine Synthesis / 2.2: |Kroehnke Pyridine Synthesis;
DOI:10.1002/chem.201203817

Reference yield:

: 1-[2-(2-fluorophenyl)-2-oxoethyl]pyridinium iodide

: 561280-12-4
C₁₉H₂₀FNO

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium acetate / acetic acid / 110 °C / Inert atmosphere

1.2: 48 h / 110 °C / Inert atmosphere

2.1: n-butyllithium; diisopropylamine / hexane; tetrahydrofuran / 2 h / -40 °C / Inert atmosphere

2.2: 20 °C / Inert atmosphere

3.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

With n-butyllithium; ammonium acetate; diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; hexane; dichloromethane; acetic acid; 1.1: |Kroehnke Pyridine Synthesis / 1.2: |Kroehnke Pyridine Synthesis;
DOI:10.1002/chem.201203817