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C28H22O6

Base Information
  • Chemical Name:C28H22O6
  • CAS No.:1111942-24-5
  • Molecular Formula:C28H22O6
  • Molecular Weight:454.479
  • Hs Code.:
C<sub>28</sub>H<sub>22</sub>O<sub>6</sub>

Synonyms:C28H22O6

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Chemical Property of C28H22O6
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Technology Process of C28H22O6

There total 12 articles about C28H22O6 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: 43.0%

Guidance literature:
With boron tribromide; In dichloromethane; at 0 - 25 ℃; for 8h; Inert atmosphere;
DOI:10.1016/j.tetlet.2011.03.002
Guidance literature:
Multi-step reaction with 5 steps
1.1: boron trifluoride diethyl etherate / dichloromethane / 40 h / 25 °C / Inert atmosphere
2.1: sodium tetrahydroborate / tetrahydrofuran; methanol / 0.5 h / 25 °C
3.1: indium(III) triflate / dichloromethane / 1 h / 25 °C / Darkness
4.1: sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.42 h / 0 - 25 °C
4.2: 12 h / 80 °C
5.1: boron tribromide / dichloromethane / 8 h / 0 - 25 °C / Inert atmosphere
With indium(III) triflate; sodium tetrahydroborate; boron trifluoride diethyl etherate; boron tribromide; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; methanol; dichloromethane; 1.1: Nazarov cyclization / 4.1: Ramberg-B?cklund olefination / 4.2: Ramberg-B?cklund olefination;
DOI:10.1016/j.tetlet.2011.03.002
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