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C23H22FNO2S

Base Information Edit
C<sub>23</sub>H<sub>22</sub>FNO<sub>2</sub>S

Synonyms:C23H22FNO2S

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C23H22FNO2S Edit
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Technology Process of C23H22FNO2S

There total 4 articles about C23H22FNO2S 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:
Guidance literature:
With potassium phosphate; 1,1'-bis(di-tertbutylphosphino)ferrocene; palladium diacetate; In ethanol; water; at 100 ℃; for 0.5h; Microwave irradiation;
DOI:10.1016/j.tetlet.2012.06.089
Guidance literature:
Multi-step reaction with 2 steps
1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
2: potassium phosphate; 1,1'-bis(di-tertbutylphosphino)ferrocene; palladium diacetate / ethanol; water / 0.5 h / 100 °C / Microwave irradiation
With potassium phosphate; 1,1'-bis(di-tertbutylphosphino)ferrocene; palladium diacetate; trifluoroacetic acid; In ethanol; dichloromethane; water; 2: Suzuki-Miyaura coupling;
DOI:10.1016/j.tetlet.2012.06.089
Guidance literature:
Multi-step reaction with 3 steps
1.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0 °C
1.2: 16 h / 20 °C
2.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
3.1: potassium phosphate; 1,1'-bis(di-tertbutylphosphino)ferrocene; palladium diacetate / ethanol; water / 0.5 h / 100 °C / Microwave irradiation
With potassium phosphate; 1,1'-bis(di-tertbutylphosphino)ferrocene; di-isopropyl azodicarboxylate; palladium diacetate; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; water; 1.1: Mitsunobu reaction / 1.2: Mitsunobu reaction / 3.1: Suzuki-Miyaura coupling;
DOI:10.1016/j.tetlet.2012.06.089
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