FloHet 2012

20
Enhanced Development and Control of Continuous Processes using Real Time In Situ FTIR Analytics Dominique Hebrault, Ph.D. Gainesville, March 5 th 2012

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Transcript of FloHet 2012

Page 1: FloHet 2012

Enhanced Development and Control of

Continuous Processes using

Real Time In Situ FTIR Analytics

Dominique Hebrault, Ph.D.

Gainesville, March 5th 2012

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For further conversation…

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Many Development & Collaboration Projects

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Continuous Chemistry - Analysis Challenges

Chemical information

- Continuous reaction monitoring superior to traditional sampling for offline

analysis (TLC, LCMS, UV, etc.)

→ Stability of reactive intermediates

→ Rapid optimization procedures

Technical knowledge

- Dispersion and diffusion: Side effects of continuous flow – must be

characterized

Today: Limited availability of convenient,

specific, in-line monitoring techniques

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In-Line IR Monitoring

Monitor Chemistry In Situ, Under Reaction Conditions

- Non-destructive

- Hazardous, air sensitive or unstable reaction species (ozonolysis, azides etc)

- Extremes in temperature or pressure

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In-Line IR Monitoring

Real-Time Analysis, “Movie” of the reaction

- Track instantaneous concentration changes (trends, endpoint, conversion)

- Minimize time delay in receiving analytical results

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In-Line IR Monitoring

Determine Reaction Kinetics, Mechanism and Pathway

- Monitor key species as a function of reaction parameters

- Track changes in structure and functional groups

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ReactIRTM Flow Cell: An Analytical Accessory

for Continuous Flow Chemical Processing

Carter, C. F.; Lange, H.; Ley, S. V.; Baxendale, I. R.; Goode, J. G.; Gaunt, N. L.; Wittkamp, B. Org. Res. Proc. Dev. 2010, 14, 393-404

In-Line FTIR Micro Flow Cell in the Laboratory

Internal volume: 10 & 50 ml

Up to 50 bar (725 psi)

-40 → 120ºC

Wetted parts: HC276, Diamond, (Silicon) & Gold

Multiplexing

Spectral range 600-4000 cm-1

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FlowIR: Flow chemistry and beyond…

Internal volume: 10 & 50 ml

Up to 50 bar (725 psi)

-40 → 120ºC

Spectral range 600-4000 cm-1

FlowIRTM: A New Plug-and-Play

Instrument for Flow Chemistry and

Beyond

9-bounce ATR sensor

(SiComp, DiComp) and head

Small size, no purge, no

alignment, no liquid N2

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The Development of Continuous Process for Alkene Ozonolysis Based

on Combined in Situ FTIR, Calorimetry, and Computational Chemistry

A Visual Method to Optimize Reaction Conditions: Case study on a

Doebner Modification of Knoevenagel Reaction

Agenda

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The Development of Continuous Process

for Alkene Ozonolysis Based on

Combined in Situ FTIR, Calorimetry, and

Computational Chemistry

Introduction

Continuous reaction setup for ozonolysis

reactions

Instantaneous “view” of the chemistry

using in situ FTIR

Investigation resulted in 2.7kg production

of API intermediate in 2 weeks

In Situ Monitoring for Continuous Manufacturing of APIs

Ayman D. Allian, Steve M. Richter, Jeffrey M. Kallemeyn, Timothy A. Robbins, and Vimal Kishore, Abbott, Process Research and Development, 1401

Sheridan Road, North Chicago, Illinois 60064, USA, Organic Process Research and Development, 2011, 15, 91-97

Steady state, rate, intermediates

Residence time (flow rate, reactor size)

O3 efficiency, mass transfer Styrene

-50°C

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In Situ Monitoring for Continuous Manufacturing of API

Ayman D. Allian, Steve M. Richter, Jeffrey M. Kallemeyn, Timothy A. Robbins, and Vimal Kishore, Abbott, Process Research and Development, 1401

Sheridan Road, North Chicago, Illinois 60064, USA, Organic Process Research and Development, 2011, 15, 91-97

xxx

(37 mmol/ sec, 2L/min)

Feed rate limited

FTIR 780 cm-1

Results

Initial lab scale kinetic study in 100ml batch

Challenges

Ozonolysis highly efficient and selective

oxidation method

Hazardous and unreliable in batch

manufacturing: Exotherm, stability of

intermediates, ozone toxicity

Styrene / MeOH / DCM

-50°C

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In Situ Monitoring for Continuous Manufacturing of API

Ayman D. Allian, Steve M. Richter, Jeffrey M. Kallemeyn, Timothy A. Robbins, and Vimal Kishore, Abbott, Process Research and Development, 1401

Sheridan Road, North Chicago, Illinois 60064, USA, Organic Process Research and Development, 2011, 15, 91-97

Results

100mL batch vessel retrofitted with

overflow valve → CSTR

Residence time distribution experiment

FTIR data confirmed by off-line HPLC

Results

Oxidation of an isobutylene-type API

intermediate

300g prod., 4d, 12h/d, 81% isol. yield

One week lead time

(Residence time distribution experiment)

Acetone (/heptane)

Rate is O3 feed-controlled

2L/min

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In Situ Monitoring for Continuous Manufacturing of API

Ayman D. Allian, Steve M. Richter, Jeffrey M. Kallemeyn, Timothy A. Robbins, and Vimal Kishore, Abbott, Process Research and Development, 1401

Sheridan Road, North Chicago, Illinois 60064, USA, Organic Process Research and Development, 2011, 15, 91-97

Results

Jacketed bubble reactor setup

32g/h – O3 generation

Applied to styrene, isobutylene-type API

intermediate

Made 2.7kg ketone, 4d, 9h/d, rate: 80g/h

2-week lead time

Conversion 99%, O3 efficiency ≈ 85%

ReactIRTM probe

Coarse frit

17L/min

-33°C

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In Situ Monitoring for Continuous Manufacturing of API

Ayman D. Allian, Steve M. Richter, Jeffrey M. Kallemeyn, Timothy A. Robbins, and Vimal Kishore, Abbott, Process Research and Development, 1401

Sheridan Road, North Chicago, Illinois 60064, USA, Organic Process Research and Development, 2011, 15, 91-97

Styrene / O3 equimolar:

Steady state 15-20% styrene

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In Situ Monitoring for Continuous Manufacturing of API

Ayman D. Allian, Steve M. Richter, Jeffrey M. Kallemeyn, Timothy A. Robbins, and Vimal Kishore, Abbott, Process Research and Development, 1401

Sheridan Road, North Chicago, Illinois 60064, USA, Organic Process Research and Development, 2011, 15, 91-97

in situ FTIR allowed to

Monitor reaction progress, detect

process upsets in real time

Ensure highest degree of product quality

and yield

Eliminate need for sampling and offline

analyses → improved productivity and

safety

Outcome

Preliminary kinetic investigation in batch

Small scale CSTR for 300g production

Larger scale continuous bubble reactor

setup for 2.7kg

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The Development of Continuous Process for Alkene Ozonolysis Based

on Combined in Situ FTIR, Calorimetry, and Computational Chemistry

A Visual Method to Optimize Reaction Conditions: Case study on a

Doebner Modification of Knoevenagel Reaction

Agenda

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Optimization of a Doebner Modification of

Knoevenagel Reaction in a Continuous

Mode

Introduction

Can reaction optimization and conditions

screening be conducted inline?

How does dispersion affect fraction

collection?

A visual method to optimize reaction conditions

Vapourtec – Flow Chemistry Solutions – Mettler Toledo collaboration project, U.K. 2011, White Paper under review

On-the-fly reaction optimization with

inline FTIR analytics

Vapourtec R2+/R4

FlowIRTM

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Results

Reference spectra of 4 main components

3 main/unique bands

7 reaction “plugs”, on-the-fly variation of

residence time and temperature (1:1.1)

Few hours experiment only

Ongoing further investigation

A visual method to optimize reaction conditions

Malonic

Acid

(1729cm-1)

Benzaldehyde

(828cm-1)

Cinnamic acid

(772cm-1)

Vapourtec – Flow Chemistry Solutions – Mettler Toledo collaboration project, U.K. 2011, White Paper under review

80°C, 10’

100°C, 10’

120°C, 20’

120°C, 10’ 100°C, 20’ 100°C, 30’

150°C, 10’

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Acknowledgements

Abbott, Process Research and Development (USA)

- Ayman D. Allian*, Steve M. Richter, Jeffrey M. Kallemeyn, Timothy A.

Robbins, and Vimal Kishore

Vapourtec Ltd. (U.K.)

- Chris Butters and Duncan Guthrie

Flow Chemistry Solutions (U.K.)

- Andrew Mansfield

Mettler Toledo Autochem

- Will Kowalchyk (USA)

- Jon Goode (U.K.)

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