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MIDA ((4-fluorophenyl)oxomethyl)boronate

Base Information Edit
  • Chemical Name:MIDA ((4-fluorophenyl)oxomethyl)boronate
  • CAS No.:1414852-71-3
  • Molecular Formula:C12H11BFNO5
  • Molecular Weight:279.032
  • Hs Code.:
  • Mol file:1414852-71-3.mol
MIDA ((4-fluorophenyl)oxomethyl)boronate

Synonyms:MIDA ((4-fluorophenyl)oxomethyl)boronate

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Chemical Property of MIDA ((4-fluorophenyl)oxomethyl)boronate Edit
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Technology Process of MIDA ((4-fluorophenyl)oxomethyl)boronate

There total 7 articles about MIDA ((4-fluorophenyl)oxomethyl)boronate 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 sodium periodate; In dichloromethane; water; at 20 ℃; for 0.166667h;
DOI:10.1016/j.tetlet.2021.153147
Guidance literature:
With Dess-Martin periodane; In dichloromethane; water; at 23 ℃;
DOI:10.1002/anie.201206501
Guidance literature:
Multi-step reaction with 5 steps
1: tricyclohexylphosphine; palladium diacetate; 2,2,2-trifluoroethanol; bromobenzene / toluene / 3 h / 60 °C / Inert atmosphere; Darkness
2: ammonium acetate; sodium periodate / acetone; water / 2 h / 80 °C / Reflux
3: toluene; dimethyl sulfoxide / 2 h / 105 °C
4: 4-methylmorpholine N-oxide; osmium(VIII) oxide / acetone; aq. phosphate buffer / 20 °C / Darkness
5: sodium periodate / dichloromethane; water / 0.17 h / 20 °C
With sodium periodate; osmium(VIII) oxide; bromobenzene; 2,2,2-trifluoroethanol; ammonium acetate; palladium diacetate; 4-methylmorpholine N-oxide; tricyclohexylphosphine; In aq. phosphate buffer; dichloromethane; water; dimethyl sulfoxide; acetone; toluene; 4: |Upjohn Dihydroxylation / 5: |Malaprade-Lemieux-Johnson Cleavage;
DOI:10.1016/j.tetlet.2021.153147
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