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2Efficient Catalytic Syntheses of Organoboronate
Esters Ubiquitous building blocks for the fine
chemical and pharmaceutical industries NORSC
Sustainable Chemistry Initiative Ramside Hall,
Durham 24th April 2012 Patrick Steel Department
of Chemistry, Durham University,
UK p.g.steel_at_durham.ac.uk
3Why make aryl boronates?
Hall, Boronic Acids, Wiley-VCH, 2nd Ed 2011
4Why make aryl boronates?
- Non-toxic
- Tolerant to air and water
- Stable in the absence of a catalyst
- React under mild conditions
- Reaction by-product is inert and benign to humans
Hall, Boronic Acids, Wiley-VCH, 2nd Ed 2011
5Classical Aryl Boronate Synthesis a Sustainable
Chemistry Challenge?
Asher et al., Tetrahedron Lett., 2003, 44, 7719
Snieckus et al., J. Org. Chem., 2009, 74, 4094
6Functional Group Tolerant Aryl Boronate Synthesis
Ishiyama, Miyaura et al., J. Org. Chem., 1995,
60, 7508
Kleeberg, Marder et al., Angew. Chem. Int. Ed.,
2009, 48, 5350
7Iridium Catalysed Arene C-H Borylation
Mkhalid, Barnard, Marder, Murphy, Hartwig, Chem.
Rev., 2010, 110, 890
8Iridium Catalysed Arene C-H Borylation
Mkhalid, Barnard, Marder, Murphy, Hartwig, Chem.
Rev., 2010, 110, 890
9Iridium Catalysed Borylation An Atom Economical
Process
10Iridium Catalysed Borylation An Atom Economical
Process
11Iridium Catalysed Borylation An Atom Economical
Process
12One-pot Transformations from Arenes
Maleczka, Smith et al., Tetrahedron, 2008, 64,
6103
Ishiyama, Miyaura et al., Tetrahedron, 2008, 64,
4967
13One-pot C-H Borylation/Suzuki-Miyaura
Cross-Coupling
Solvent Temp ( C) Time (h) GC-MS Conversion ()
DMF 80 6 0
1,4-dioxane 80 6 25
MeCN 80 6 37
2-MeTHF 80 6 85
MTBE 80 6 100
Peter Harrisson
14One-pot C-H Borylation/Suzuki-Miyaura
Cross-Coupling
Peter Harrisson
15One-pot C-H Borylation/Suzuki-Miyaura
Cross-Coupling
Peter Harrisson
16One-pot C-H Borylation/Suzuki-Miyaura
Cross-Coupling
Peter Harrisson
17One-pot C-H Borylation/Suzuki-Miyaura
Cross-Coupling
Peter Harrisson
18Microwave Accelerated One-Pot Biaryl Synthesis
Peter Harrisson
19Challenges for Ir-Catalysed Arene C-H
Borylation Regiocontrol
20Challenges for Ir-Catalysed Arene C-H
Borylation Heterocyclic Organoboronic Acids
Data Courtesy David Blakemore Pfizer - Neusentis
21Challenges for the Synthesis of Heterocyclic
Boronate Esters
22Challenges for the Synthesis of Heterocyclic
Boronate Esters
23Quinoline Boronate Esters
Peter Harrisson
24Where Now for Cleaner Greener Aromatic C-H
Borylation?
Other sequential chemistries Faster more
effective Catalysts. Better ligand sets to
control regiochemistry.
25Where Now for Cleaner Greener Aromatic C-H
Borylation?
26Where Now for Cleaner Greener Aromatic C-H
Borylation?
Other sequential chemistries Faster more
effective Catalysts. Better ligand sets to
control regiochemistry. Cheaper metals than Ir
Cu????
27Alkyl Boronate Esters via Cu-Catalysed C-X
Activation
Hazmi Tajuddin
282012 Durham Lectures
Prof John Hartwig University of California,
Berkeley
Monday 14th May Tuesday 15th May Wednesday 16th
May Department of Chemistry, Durham
University All Lectures Commence at 4pm
Visitors Welcome For Further Details
p.g.steel_at_durham.ac.uk
29Understanding and Optimising Chemical Processes
2nd 3rd July 2012 Department of
Chemistry Durham University
This two-day programme provides delegates with an
opportunity to augment their process knowledge
using Principal Components Analysis (PCA) and
Design of Experiments (DoE) methodologies to
expand process understanding, establish and
develop capability, ensure robust and in-control
processes, improve quality and reduce operational
and environmental costs.
Keynote Speaker Martin Owen Product Development,
GlaxoSmithKline, Stevenage
Further Information Registration Contact
Matthew Linsley, ISRU, Newcastle
University matthew.linsley_at_newcastle.ac.uk
30Acknowledgements
Prof Todd Marder
Peter Harrisson Hazmi Tajuddin Bianca
Bitterlich Prof Lei Liu (Tsinghua University,
Beijing)
James Morris (Syngenta) Aoife Maxwell (GSK) Lena
Shukla (GSK)
Alan Kenwright (NMR) Jackie Mosely (MS) Andrei
Batsanov (X-ray)
31Understanding and Optimising Chemical Processes
2nd 3rd July 2012 Department of
Chemistry Durham University
This two-day programme provides delegates with an
opportunity to augment their process knowledge
using Principal Components Analysis (PCA) and
Design of Experiments (DoE) methodologies to
expand process understanding, establish and
develop capability, ensure robust and in-control
processes, improve quality and reduce operational
and environmental costs.
Keynote Speaker Martin Owen Product Development,
GlaxoSmithKline, Stevenage
Further Information Registration Contact
Matthew Linsley, ISRU, Newcastle
University matthew.linsley_at_newcastle.ac.uk
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