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C48H44F2O7

Base Information Edit
C<sub>48</sub>H<sub>44</sub>F<sub>2</sub>O<sub>7</sub>

Synonyms:C48H44F2O7

Suppliers and Price of C48H44F2O7
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C48H44F2O7 Edit
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Technology Process of C48H44F2O7

There total 5 articles about C48H44F2O7 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 n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; Inert atmosphere;
Guidance literature:
Multi-step reaction with 5 steps
1.1: diethylamino-sulfur trifluoride / methanol / dichloromethane / 20 °C / Inert atmosphere
2.1: n-butyllithium / tetrahydrofuran / 0.17 h / -78 °C / Inert atmosphere
2.2: -78 °C / Inert atmosphere
3.1: tetrahydrofuran; diisobutyl ether / 1 h / -78 °C / Inert atmosphere
4.1: N-Bromosuccinimide / tetrachloromethane / 15 h / Inert atmosphere; UV-irradiation; Reflux
5.1: n-butyllithium / tetrahydrofuran; hexane / -78 °C / Inert atmosphere
With N-Bromosuccinimide; n-butyllithium; diethylamino-sulfur trifluoride; methanol; In tetrahydrofuran; tetrachloromethane; hexane; dichloromethane; diisobutyl ether; 5.1: Barbier Reaction;
Guidance literature:
Multi-step reaction with 4 steps
1.1: n-butyllithium / tetrahydrofuran / 0.17 h / -78 °C / Inert atmosphere
1.2: -78 °C / Inert atmosphere
2.1: tetrahydrofuran; diisobutyl ether / 1 h / -78 °C / Inert atmosphere
3.1: N-Bromosuccinimide / tetrachloromethane / 15 h / Inert atmosphere; UV-irradiation; Reflux
4.1: n-butyllithium / tetrahydrofuran; hexane / -78 °C / Inert atmosphere
With N-Bromosuccinimide; n-butyllithium; In tetrahydrofuran; tetrachloromethane; hexane; diisobutyl ether; 4.1: Barbier Reaction;
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