Practical Process Research and Development
A Guide for Organic Chemists
- 3rd Edition - May 1, 2026
- Latest edition
- Author: Neal G. Anderson
- Language: English
- Paperback ISBN:9 7 8 - 0 - 4 4 3 - 3 6 5 2 2 - 5
- eBook ISBN:9 7 8 - 0 - 4 4 3 - 3 6 5 2 3 - 2
Practical Process Research and Development: A Guide for Organic Chemists, Third Edition provides a concise, comprehensive, step-by-step framework to support understanding and im… Read more
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Practical Process Research and Development: A Guide for Organic Chemists, Third Edition provides a concise, comprehensive, step-by-step framework to support understanding and implement organic process research and development in the pharmaceutical, fine chemical, and agricultural chemical industries. Neal G. Anderson has heavily updated the book once again for its third edition, whilst retaining the basic spirit and structure of the first two editions. The book describes the steps taken following synthesis and evaluation to bring key compounds to market in a cost-effective manner. He describes hands-on, step-by-step, approaches to solving process development problems, including route, reagent, and solvent selection, optimising catalytic reactions, chiral syntheses, and green chemistry. Practical Process Research and Development: A Guide for Organic Chemists, Third Edition is written primarily for organic, medicinal, pharmaceutical, and chemical process development chemists as well as chemical engineers- it is well suited for beginners at upper undergraduate and graduate student level and early career researchers who need an accessible insight into industrial process R&D.
- Reflects the current thinking in chemical process R&D for small molecules
- Provides insights into generating rugged, practical, cost-effective processes for the chemical preparation of small molecules
- Breaks down process optimization into route, reagent and solvent selection, development of reaction conditions, workup, crystallizations and more
- Presents guidelines for implementing and troubleshooting critical processes
- Includes various problem sets, providing readers with the opportunity to reflect on the course material and real-life situations that
- Provides a framework for practical chemical process development for those new to industry, and to provide examples to aid researchers who have been conducting industrial process R&D
Organic, medicinal, pharmaceutical, and chemical process development chemists, as well as chemical engineers. It is well suited for beginners at upper undergraduate and graduate student level and early career researchers who need an accessible insight into industrial process R&D
Foreword Preface
1. Introduction
2. Safety Reactions
3. Route selection
4. Reagent selection
5. Solvent selection
6. Practical considerations for scale-up
7. In-process controls and reaction duration
8. Process optimization by minimizing impurities
9. Work-up conditions
10. Purification, crystallization and isolation
11. Final product form and impurities
12. Continuous operations
13. Scale-up concerns, validation, and process implementation
14. Trouble-shooting
1. Introduction
2. Safety Reactions
3. Route selection
4. Reagent selection
5. Solvent selection
6. Practical considerations for scale-up
7. In-process controls and reaction duration
8. Process optimization by minimizing impurities
9. Work-up conditions
10. Purification, crystallization and isolation
11. Final product form and impurities
12. Continuous operations
13. Scale-up concerns, validation, and process implementation
14. Trouble-shooting
- Edition: 3
- Latest edition
- Published: May 1, 2026
- Language: English
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Neal G. Anderson
Neal G. Anderson is a synthetic organic chemist with over 40 years of experience in chemical process R&D in the pharmaceutical industry. He earned a B.S. degree in biology from the University of Illinois and a Ph.D. in medicinal chemistry from the University of Michigan, followed by industrial post-doctoral studies at McNeil Laboratories. He has extensive hands-on experience in the laboratory, pilot plant, and in manufacturing facilities. At Squibb / Bristol-Myers Squibb he made key contributions to processes for the manufacture of four major drug substances, including captopril, and has participated in 12 manufacturing start-ups and introductions of many processes to pilot plants. He received a BMS President's Award and spot awards, and his final position was Principal Scientist. In 1997, Anderson established Anderson’s Process Solutions L.L.C., a consulting firm based in the USA to offer practical guidance on developing and implementing processes for bulk pharmaceuticals and fine chemicals. As part of these consulting services, he presents courses on selected aspects of practical process R&D. He is experienced in laboratory research, scale-up, and technology transfer to ensure reproducibility and optimal product quality.
Affiliations and expertise
Anderson's Process Solutions LLC, USA