4.6 Article

Green hydroboration of carboxylic acids and mechanism investigation

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 17, Issue 14, Pages 3604-3608

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ob00485h

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Funding

  1. National Natural Science Foundation of China [21772093]
  2. Natural Science Foundation of Jiangsu Province, China [BK20181421]
  3. Postgraduate Research AMP
  4. Practice Innovation Program of Jiangsu Province [KYCX17_0846]
  5. Doctorate Fellowship Foundation of Nanjing Forestry University [163360767]
  6. PAPD

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A catalyst-free and solvent-free method for the hydroboration of a variety of carboxylic acids with pinacolborane was developed. The hydroboration of various aromatic and aliphatic carboxylic acids as well as dicarboxylic acids with HBpin could be completed within 6 h at room temperature or within 1 h at 60 degrees C to give the products in quantitative yields under neat conditions without the need for any solvent or metal catalyst. The possible reaction mechanism was investigated in detail based on the corresponding DFT calculations and the stoichiometric reaction of acetic acid with different equivalents of HBpin (at room temperature and 0 degrees C) and it revealed the stepwise nature of the protocol.

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