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Mutli step synthesis

Synthesis of sulfanilamide

Objective

In this lab we will synthesize sulfanilamide starting with aniline. Our synthetic steps will include a protection of an amine, followed by chlorosulfonylation of the protected aniline. This compound is then deprotected and converted to our target molecule, sulfanilamide, in one final step.

Grading

You will be assessed on:

  • Write-up in your Lab Notebook
  • TA evaluation of lab procedure
  • Answers to Post Lab questions

Introduction

Sulfa drugs have been a very integral part of our medical history. Sulfa drugs were first used in the 1930’s, and are now the oldest antibiotics available and also among the best. Sulfa compounds work by inhibiting nucleic acid (DNA, RNA) synthesis. The way sulfa compounds work is by shutting down the system by which bacteria synthesize their folic acid. They do this by competing with para-aminobenzoic acid (PABA, necessary for folic acid synthesis). See Figure 1 to see if you can tell why sulfanilamide is a competitor for PABA.

Experimental

1. Place 5mL conical vial, Claisen head,½dram vial, and a drying tube packed with glass wool and calcium chloride into the oven for 30 minutes at 125 ° C size 12{°C} {} . 2. Remove glassware from oven and allow it to cool.3. Measure out 230 μL size 12{μL} {} of aniline and 500 μL size 12{μL} {} of methylene chloride to the 5mL conical vial. 4. Immediately place the Claisen head equipped with a septum cap and the drying tube to the vial.5. Place the setup in an ice bath to cool the reagents before adding trifluoroacetic acid. 6. Once the reagents are cool (5 minutes), add 500 μL size 12{μL} {} of methylene chloride to a½dram vial. To this then add 500 μL size 12{μL} {} of trifluoroacetic acid. Draw up the 1 mL total of solution into a syringe and add it through the septum dropwise to the aniline solution.Note: The reaction is exothermic, if the addition is too rapid, the methylene chloride will evaporate. 7. After the addition is complete, let reaction stand at room temperature for 10 minutes.8. After reaction is at room temperature, remove the claisen head and remove methylene chloride by passing air over the top of the solution. This will evaporate the methylene chloride and residual trifluoroacetic acid, leaving the product as a white powder.

Next

1. Place an air condenser and a 9-in Pasteur pipet calibrated to deliver 0.9 mL, into the oven for 30 minutes at 125 ° C size 12{°C} {} .2. Remove glassware from oven and allow it to cool.3. Attach the vial containing 2,2,2-trifluoracetanilide to the dry air condenser.4. Measure out 0.9 mL of chlorosulfonic acid with the pipet and slowly add it to the vial by inserting the pipet down the air condenser.5. Place vial with condenser attached into a sand bath and heat for 10 min. at 65 ° C size 12{°C} {} .6. Collect the precipitate by vacuum filtration and wash with three 1-mL portions of cold water.7. Let the product air dry. Determine the melting point and overall yield.8. Weigh out 400 mg of the p-(2,2,2-trifluoroacetamido)benzenesulfonyl chloride into a 10-mL Erlenmeyer flask.9. In a test tube measure out 0.6 mL of concentrated ammonium hydroxide and 0.4 mL deionized water.10. Add the ammonium hydroxide solution to the Erlenmeyer containing the p-(2,2,2-trifluoroacetamido)benzenesulfonyl chloride. Use a glass stirring rod to break up any chunks that form.11. Add a boiling stone to the Erlenmeyer flask and place the reaction mixture into a sand bath. Heat the reaction to boiling and watch for all the solid to dissolve. Once total dissolution has occurred boil the mixture for an additional minute.12. Once reaction is complete remove the flask from the sand bath and allow to cool to room temperature. Once this is done place the flask into an ice bath for 15 min.13. Collect the yellow crystals that precipitate out of solution and isolate them via vacuum filtration. Wash with three 0.5 mL portions of water to remove any soluble impurities.14. Let the product air dry. Determine the melting point and overall yield.

Post-lab questions:

1. Who won the Nobel Prize for the discovery of sulfanilamide drugs?

2. To give you a better idea of the massive amount and diversity of protecting groups, assign structures to the following list of protecting group abbreviations:AcAdBnBOCCbzFmocMEMONBPptTBDMSTfTHPTIPSTMSTos

A good ref. Protective Groups in Organic Synthesis by Theodora W. Greene3. How do sulfa drugs work?

4. Draw a mechanistic scheme for all reactions done in this lab. (Show correct arrow pushing, and mechanistic detail.)

Questions & Answers

who was the first nanotechnologist
Lizzy Reply
k
Veysel
technologist's thinker father is Richard Feynman but the literature first user scientist Nario Tagunichi.
Veysel
Norio Taniguchi
puvananathan
Interesting
Andr
I need help
Richard
anyone have book of Abdel Salam Hamdy Makhlouf book in pdf Fundamentals of Nanoparticles: Classifications, Synthesis
Naeem Reply
what happen with The nano material on The deep space.?
pedro Reply
It could change the whole space science.
puvananathan
the characteristics of nano materials can be studied by solving which equation?
sibaram Reply
plz answer fast
sibaram
synthesis of nano materials by chemical reaction taking place in aqueous solvents under high temperature and pressure is call?
sibaram
hydrothermal synthesis
ISHFAQ
how can chip be made from sand
Eke Reply
is this allso about nanoscale material
Almas
are nano particles real
Missy Reply
yeah
Joseph
Hello, if I study Physics teacher in bachelor, can I study Nanotechnology in master?
Lale Reply
no can't
Lohitha
where is the latest information on a no technology how can I find it
William
currently
William
where we get a research paper on Nano chemistry....?
Maira Reply
nanopartical of organic/inorganic / physical chemistry , pdf / thesis / review
Ali
what are the products of Nano chemistry?
Maira Reply
There are lots of products of nano chemistry... Like nano coatings.....carbon fiber.. And lots of others..
learn
Even nanotechnology is pretty much all about chemistry... Its the chemistry on quantum or atomic level
learn
Google
da
no nanotechnology is also a part of physics and maths it requires angle formulas and some pressure regarding concepts
Bhagvanji
hey
Giriraj
Preparation and Applications of Nanomaterial for Drug Delivery
Hafiz Reply
revolt
da
Application of nanotechnology in medicine
has a lot of application modern world
Kamaluddeen
yes
narayan
what is variations in raman spectra for nanomaterials
Jyoti Reply
ya I also want to know the raman spectra
Bhagvanji
I only see partial conversation and what's the question here!
Crow Reply
what about nanotechnology for water purification
RAW Reply
please someone correct me if I'm wrong but I think one can use nanoparticles, specially silver nanoparticles for water treatment.
Damian
yes that's correct
Professor
I think
Professor
Nasa has use it in the 60's, copper as water purification in the moon travel.
Alexandre
nanocopper obvius
Alexandre
what is the stm
Brian Reply
is there industrial application of fullrenes. What is the method to prepare fullrene on large scale.?
Rafiq
industrial application...? mmm I think on the medical side as drug carrier, but you should go deeper on your research, I may be wrong
Damian
STM - Scanning Tunneling Microscope.
puvananathan
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Source:  OpenStax, Chem 215 spring08. OpenStax CNX. Mar 21, 2008 Download for free at http://cnx.org/content/col10496/1.8
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