C₂₃H₂₁FN₂O₂

Base Information

Chemical Name:C₂₃H₂₁FN₂O₂
CAS No.:1208870-96-5
Molecular Formula:C₂₃H₂₁FN₂O₂
Molecular Weight:376.43
Hs Code.:

C<sub>23</sub>H<sub>21</sub>FN<sub>2</sub>O<sub>2</sub>

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₃H₂₁FN₂O₂

Chemical Property:

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Technology Process of C₂₃H₂₁FN₂O₂

There total 5 articles about C₂₃H₂₁FN₂O₂ 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:

: 1208318-11-9
4-(2-formyl-1H-pyrrol-1-yl)-3-methylbenzonitrile

: 1208870-96-5
C₂₃H₂₁FN₂O₂

Guidance literature:: Multi-step reaction with 4 steps

1: toluene / Reflux

2: palladium 10% on activated carbon; hydrogen / ethanol

3: N-Bromosuccinimide

4: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; sodium carbonate; In ethanol; toluene; 1: Wittig reaction / 4: Suzuki coupling;
DOI:10.1021/ml200045s

Reference yield:

: 106037-36-9
4-amino-3-methylbenzamide

: 1208870-96-5
C₂₃H₂₁FN₂O₂

Guidance literature:: Multi-step reaction with 6 steps

1: acetic acid

2: trichlorophosphate

3: toluene / Reflux

4: palladium 10% on activated carbon; hydrogen / ethanol

5: N-Bromosuccinimide

6: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; sodium carbonate; acetic acid; trichlorophosphate; In ethanol; toluene; 2: Vilsmeier formylation / 3: Wittig reaction / 6: Suzuki coupling;
DOI:10.1021/ml200045s

Reference yield:

: 1208318-10-8
3-methyl-4-(1H-pyrrol-1-yl)benzamide

: 1208870-96-5
C₂₃H₂₁FN₂O₂

Guidance literature:: Multi-step reaction with 5 steps

1: trichlorophosphate

2: toluene / Reflux

3: palladium 10% on activated carbon; hydrogen / ethanol

4: N-Bromosuccinimide

5: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; sodium carbonate; trichlorophosphate; In ethanol; toluene; 1: Vilsmeier formylation / 2: Wittig reaction / 5: Suzuki coupling;
DOI:10.1021/ml200045s