Difference between revisions of "Synthesis and Characterization of Lignin Monomers"

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[https://www.sigmaaldrich.com/catalog/product/aldrich/d7927?lang=en&region=US Sinapic acid]
 
[https://www.sigmaaldrich.com/catalog/product/aldrich/d7927?lang=en&region=US Sinapic acid]
  
==Synthesis==
+
Ethanol
*'''Ethyl Ferulate:''' 10 g of ferulic acid dissolved in 100 mL ethanol and 5 mL of acetyl chloride. Solution stirred overnight. Volatiles removed by rotary evaporation (rotovap) at 40 C. (Ralph)
 
*'''Esterification:''' 0.36 M ferulic acid in ethanol (500 mL) with concentrated HCl. Refluxed for two days. Cooled and ethanol evaporated under pressure (rotovap). Crude extract combined with ethyl acetate (250 mL). Solution dried over anhydrous MgSO<sub>4</sub>.
 
  
===Synthesis Mechanism===
+
Acetyl Chloride
  
=Results=
+
===Safety===
  
[[File:HPLC Data.jpg|600px|right]]
+
==Experimental Procedures==
  
-
+
Preparation of 2 mM Ferulic Acid Standards
 +
* 100 mL solution is made with pH 5 buffer using deionized water
 +
* 0.0385 g of Ferulic Acid added to pH 5 buffer
  
-
+
Preparation through 8--5 Coupled Diferulate Procedure ()
 +
*'''Ethyl Ferulate:''' 10 g of ferulic acid dissolved in 100 mL ethanol and 5 mL of acetyl chloride. Solution stirred overnight. Volatiles removed by rotary evaporation (rotovap) at 40 C.
 +
* '''Dimerization:''' Product of ethyl ferulate dissolved in pH 4.0 acetate buffer. Solution is cooled and added to peroxidase(10 mg in 2 mL of phosphate buffer). Product filtered out to obtain crude product.
 +
* '''Purification:''' Use of flash chromatography with EtOAc as eluant. Product recrystallized allowing for NMR data and melting point.
 +
[[File:IMG_2031.JPG|300px|right]]
 +
Preparation_________
  
-
+
*'''Esterification:''' 0.36 M ferulic acid in ethanol (500 mL) with concentrated HCl. Refluxed for two days. Cooled and ethanol evaporated under pressure (rotovap). Crude extract combined with ethyl acetate (250 mL). Solution dried over anhydrous MgSO<sub>4</sub>.
  
-
+
===Synthesis Mechanism===
  
-
+
=Results=
  
-
+
While minimal research was able to be accomplished, discussion on methods were able to be looked at to finding a more green chemistry approach. The initial method allowed for a two day reflux accumulating in a significant amount of water being used (roughly 700+ gallons). Producing the ferulic acid standard is used in HPLC analysis. Running samples of standards and product from experimental procedures through the HPLC instrument looking at the intensity over a retention time of 30 minutes.
  
-
+
[[File:HPLC Data.jpg|400px]] [[File:Screenshot (2).png|400px]]
  
 
=Discusion=
 
=Discusion=
  
 
=Conclusion=
 
=Conclusion=
 +
 +
Through more compassion between procedures would allow for a more green approach in a laboratory setting. With the possibility of a microwave reactor would allow for lignin synthesis to be rapidly produced.
  
 
== References ==
 
== References ==
  
*[https://pubs.acs.org/doi/abs/10.1021/jf980123r Simple Preparation of 8--5-coupled Diferulate]
+
1. [[https://books.google.com/books?hl=en&lr=&id=E74LS-rm6t8C&oi=fnd&pg=PP1&dq=lignin+and+lignans+advances+in+chemistry+overview&ots=CAXGjH-1vt&sig=i4mXAsF5VhIWhelYS7AUhr5virg#v=onepage&q&f=false| Overview from ''Lignin and Lignans: Advances in Chemistry'']]
  
*[https://pubs.acs.org/doi/abs/10.1021/acssuschemeng.5b01281 Structure-Activity Relationships]
+
2. [[Media:Lignin biosynthesis and Structure.pdf|Lignin Biosynthesis and Structure]]
  
*[[Media:Lignin biosynthesis and Structure.pdf|Lignin Biosynthesis and Structure]]
+
3. [[Media:Lignin ref Burkit.pdf|Oxidative Coupling during Lignin Polymerization is Determined by Unpaired Electron Delocalization within Parent Phenylpropanoid Radicals]]
  
*[[Media:Lignin ref Burkit.pdf|Oxidative Coupling during Lignin Polymerization is Determined by Unpaired Electron Delocalization within Parent Phenylpropanoid Radicals]]
+
4. [[Media:Alcohol synthesis procedure.pdf|Facile Large-Scale Synthesis of Coniferyl, Sinapyl, and p-Coumaryl Alcohol]]
  
*[[https://books.google.com/books?hl=en&lr=&id=E74LS-rm6t8C&oi=fnd&pg=PP1&dq=lignin+and+lignans+advances+in+chemistry+overview&ots=CAXGjH-1vt&sig=i4mXAsF5VhIWhelYS7AUhr5virg#v=onepage&q&f=false| Overview from ''Lignin and Lignans: Advances in Chemistry'']]
+
5. [https://pubs.acs.org/doi/abs/10.1021/jf980123r Simple Preparation of 8--5-coupled Diferulate]
 +
*PDF Version: [[:File:Simple Preparation of 8-5 Coupled Diferu.pdf]]
  
*[[Media:Alcohol synthesis procedure.pdf|Facile Large-Scale Synthesis of Coniferyl, Sinapyl, and p-Coumaryl Alcohol]]
+
6. [https://pubs.acs.org/doi/abs/10.1021/acssuschemeng.5b01281 Structure-Activity Relationships]
 +
*PDF Version: [[:File:Structure-Activity Relationships.pdf]]

Latest revision as of 23:00, 14 May 2020

Prior research on Synthesis of Lignin Monomers done by: Alexandria N. Tibbs

Abstract

Lignin is the second most abundant organic polymer. The structure of lignin is composed of three monomers: p-coumaryl alcohol, coniferyl alcohol, and sinapyl alcohol, which all are found in nature. These natural compounds are not cost friendly for undergraduate research. The carboxylic acid forms of these monomers (p-coumaric acid, ferulic acid, and sinapic acid) can be obtained commercially. This poster will discuss our synthetic approaches to produce the alcohol forms of lignin.

Lignin Monomers

p-Coumaryl alcohol

Lignin Precursors

P-Coumaryl alcohol.svg.png

Coniferyl alcohol

Coniferol.svg.png

Sinapyl alcohol

Sinapyl alcohol.svg.png

Introduction

Ferulates play important roles in plant growth and undergo radical coupling reactions to produce dimers and cross-linking. Significant quantities are now required by cell wall researchers increasing the the large scale production of these ferulates and other lignins similar to their make up.

Methods/Experimentation

Materials

Ferulic acid

p-Coumaric acid

Sinapic acid

Ethanol

Acetyl Chloride

Safety

Experimental Procedures

Preparation of 2 mM Ferulic Acid Standards

  • 100 mL solution is made with pH 5 buffer using deionized water
  • 0.0385 g of Ferulic Acid added to pH 5 buffer

Preparation through 8--5 Coupled Diferulate Procedure ()

  • Ethyl Ferulate: 10 g of ferulic acid dissolved in 100 mL ethanol and 5 mL of acetyl chloride. Solution stirred overnight. Volatiles removed by rotary evaporation (rotovap) at 40 C.
  • Dimerization: Product of ethyl ferulate dissolved in pH 4.0 acetate buffer. Solution is cooled and added to peroxidase(10 mg in 2 mL of phosphate buffer). Product filtered out to obtain crude product.
  • Purification: Use of flash chromatography with EtOAc as eluant. Product recrystallized allowing for NMR data and melting point.
IMG 2031.JPG

Preparation_________

  • Esterification: 0.36 M ferulic acid in ethanol (500 mL) with concentrated HCl. Refluxed for two days. Cooled and ethanol evaporated under pressure (rotovap). Crude extract combined with ethyl acetate (250 mL). Solution dried over anhydrous MgSO4.

Synthesis Mechanism

Results

While minimal research was able to be accomplished, discussion on methods were able to be looked at to finding a more green chemistry approach. The initial method allowed for a two day reflux accumulating in a significant amount of water being used (roughly 700+ gallons). Producing the ferulic acid standard is used in HPLC analysis. Running samples of standards and product from experimental procedures through the HPLC instrument looking at the intensity over a retention time of 30 minutes.

HPLC Data.jpg Screenshot (2).png

Discusion

Conclusion

Through more compassion between procedures would allow for a more green approach in a laboratory setting. With the possibility of a microwave reactor would allow for lignin synthesis to be rapidly produced.

References

1. [Overview from Lignin and Lignans: Advances in Chemistry]

2. Lignin Biosynthesis and Structure

3. Oxidative Coupling during Lignin Polymerization is Determined by Unpaired Electron Delocalization within Parent Phenylpropanoid Radicals

4. Facile Large-Scale Synthesis of Coniferyl, Sinapyl, and p-Coumaryl Alcohol

5. Simple Preparation of 8--5-coupled Diferulate

6. Structure-Activity Relationships