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Experiment 20

Experiment 20. CHEMOSELECTIVE REDUCTION WITH NaBH 4. Objectives:. To synthesize vanillin acetate by acetylation of p-vanillin, then to perform a chemoselective reduction using NaBH 4 . To use TLC to follow the course of the reaction.

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Experiment 20

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  1. Experiment 20 CHEMOSELECTIVE REDUCTION WITH NaBH4

  2. Objectives: • To synthesize vanillin acetate by acetylation of p-vanillin, then to perform a chemoselective reduction using NaBH4. • To use TLC to follow the course of the reaction. • To analyzethe purity of products using TLC, HPLC and melting point analysis. • To characterize the reactants and products using 1H-NMR and IR spectroscopy.

  3. Before coming to lab… • Review these techniques: • Vacuum filtration • TLC Analysis • HPLC analysis • Melting point analysis • Extraction

  4. CHEMICAL EQUATION(Acetylation)

  5. MECHANISM(Acetylation)

  6. OVERVIEW(Part 1) • Synthesize vanillin acetate. • Isolate solid product using vacuum filtration, or oily product by extraction. • Prepare HPLC sample of pure product and submit for analysis. • Perform TLC experiment on pure product. • Secure product and allow to dry until next lab period.

  7. SYNTHESIS(Preparation of Vanillin Acetate) • Mix p-vanillin and aqueous NaOH in flask with stir bar. • Add ice, then acetic anhydride drop wise. • Cover loosely with cork, then stir 15 minutes. 125 mL

  8. PURIFICATION(Preparation of Vanillin Acetate) • If a white solid forms… • Suction filter • Recrystallize with ethanol • Cool to room temp, then in ice bath • Suction filter again • Prepare HPLC and TLC samples (LABEL CLEARLY!) • Submit solid product to instructor to dry until next lab period.

  9. PURIFICATION(Preparation of Vanillin Acetate) • If an oil forms… • Transfer to separatory funnel and extract 2X with ethyl acetate. • Wash organic layer with aqueous NaOH and check pH. • Dry over MgSO4. • Evaporate solvent. • Prepare HPLC and TLC samples (LABEL CLEARLY!) • Submit solid product to instructor to dry until next lab period.

  10. Tables 20.1 and 20.3

  11. SAFETY • Acetic anhydride and NaOH are both corrosive! • Ethanol is highly flammable!

  12. WASTE • LIQUID WASTE: Place liquid filtrate from vacuum filtration in this container.

  13. CHEMICAL EQUATION(Reduction) *NOTE*Stoichiometry for this reaction is 4:1. This means that 1 mole of NaBH4 can reduce 4 moles of carbonyl compound, to produce 4 moles of the product.

  14. REDUCING AGENTS • Reducing agents cause a reaction resulting in a product containing more bonds from carbon to hydrogen (or fewer bonds to oxygen). • NaBH4 (sodium borohydride) is a versatile and useful reducing agent in organic chemistry, however will only reduce carbonyl groups of aldehydes and ketones. • LAH (lithium aluminum hydride) is another common reducing agent, however use of this reducing agent will result in the reduction of many other carbonyl containing compounds, including esters, carboxylic acids and amides.

  15. MECHANISM(Reduction)

  16. OVERVIEW(Part 2) • Reweigh ACYLATION PRODUCT, perform melting point analysis. • Cool, then react with NaBH4 in ethanol. • TLC @ 30min to determine reaction progress. • If complete, transfer to sep funnel. • Perform extraction, dry organic layer. • Evaporate solvent, obtain product mass. • Submit HPLC samples for analysis. • Perform final TLC analysis and stain in 2,4-DNP.

  17. SYNTHESIS(Reduction) • Reweigh solid product from previous lab, calculate % yield, and obtain mp. • Transfer solid to flask w/stir bar and dissolve in ethanol. • Cool in ice bath, then slowly add NaBH4 while stirring. • Stir at 0oC for 15 min, then 15 min more at RT. • Perform TLC experiment to determine reaction progress. • If complete, add 10 mL water and stir 5 minutes. 50 mL

  18. PURIFICATION(Reduction) • Transfer reaction solution to separatory funnel. • Extract 2X with diethyl ether. • Wash with water and brine. • Dry organic layer over MgSO4. • Decant liquid ONLY into tared flask and evaporate solvent. • Obtain product mass & calculate % yield. • Prepare HPLC and TLC samples.

  19. Tables 20.2 and 20.4

  20. PRODUCT ANALYSIS—HPLC • HPLC Analysis • Used at the end of the experiment to identify and quantify compounds present during the synthesis, as well as the purity of the final products from each step. • Table 20.5:

  21. PRODUCT ANALYSIS—TLC • TLC Analysis • Used to determine reaction progress during the course of the experiment, as well as to identify and determine purity of products at the end of the experiment. • 2,4-DNP will be used as a stain to detect the presence/absence of the aldehyde functional group. • Table 20.6:

  22. PRODUCT ANALYSIS—IR • IR Analysis • IR spectra of reactants and products can be used to determine the presence and absence of certain types of functional groups which indicate the conversion of one compound to another during the course of the synthesis. • Table 20.7:

  23. PRODUCT ANALYSIS—NMR • NMR Analysis • 1H-NMR spectra of reactants and products can be used to determine the presence and absence of certain types of signals which indicate the conversion of one compound to another during the course of the synthesis. • Table 20.8:

  24. SAFETY CONCERNS • Ethanol, ethyl acetate, hexane, diethyl ether, and acetone are all FLAMMABLE materials. • Sodium borohydride and 2,4-DNP are TOXICin large concentrations. • Sulfuric acid, used to prepare 2,4-DNP stain, is CORROSIVE.

  25. WASTE MANAGEMENT • SOLID WASTE: Place all solid waste in this container including magnesium sulfate or any solid product. • LIQUID WASTE : Place all liquid waste into this container including filtrates and aqueous washes from extraction. • GLASS WASTE: Place used TLC and melting point capillary tubes in this container. • PAPER WASTE: Place any gloves, TLC plates, filter papers, paper towels, etc. in the yellow trashcan.

  26. CLEANING • Any glassware used to contain only volatile organic solvents can simply be rinsed with wash acetone. • All other glassware should be cleaned with soap, water and brush, then rinsed with wash acetone or hand dried.

  27. LABORATORY NOTEBOOK(Pre-lab) • OBJECTIVE(Must clearly state…) • What compounds will be made and how • What will be investigated with the compounds • CHEMICAL EQUATION • Include the general chemical equation from the top of page 169 from handout. • TABLE OF PHYSICAL DATA (Complete the following table using a site listed on WWW Links ONLY. Wikipedia is unacceptable!) • REFERENCE TO PROCEDURE (Must include…) • full title including edition and author names • numbers where actual procedure can be found

  28. LABORATORY NOTEBOOK(In-lab—Part 1) • Synthesis: Preparation of Vanillin Acetate • Weight of p-vanillin used • Weight of ice used • Volume of 10% NaOH used • Volume of acetic anhydride used • Theoretical yield calculation • Purification of Vanillin Acetate • Volume ethanol used • Weight of small filter • Weight of watch glass • HPLC vial slot # of ACYLATION PRODUCT • Weight of filter + watch glass + dry product • Final product mass • % yield calculation • Experimental melting point • Atom economy calculation • Experimental atom economy calculation • “Eproduct” calculation • Cost per synthesis calculation • Cost per gram calculation

  29. LABORATORY NOTEBOOK(In-lab—Part 2) • Synthesis: Reduction of Vanillin Acetate • Volume of ethanol used • Weight of sodium borohydride used • Sketch of TLC diagram (taken during experiment) • Theoretical yield calculation (based on product mass from part 1!) • Purification of Product Alcohol • Volume of diethyl ether, deionized water, and NaCl used • HPLC vial slot # of PURE REDUCTION PRODUCT • Weight of 50 mL flask • Weight of flask + product • Final product mass • % yield, Atom economy, Experimental atom economy, “Eproduct”, Cost per synthesis, and Cost per gram calculations • Sketch of TLC diagram (taken at end of experiment) • EXPERIMENTAL PROCEDURE • In paragraph form, BRIEFLY describe the procedure that you actually followed during the lab. • Paragraph must be written in PAST TENSE, PASSIVE VOICE. • Include any volumes or weights of chemicals used during the experiment. • Include any mistakes, accidents or observations if applicable.

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