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The third step of the lidocaine project actually synthesizes the lidocaine using the chloroanilide and diethylamine. Here are a few pointers:
It is important that the anilide and the glassware used in the experiment are dry. Why?
If needed, the reflux time can be shortened to about 75 minutes. The hoses have to be properly attached so that they do not detach from the water jacketed condenser during the reflux period, which is often times unsupervised (due to the characterization of the previous compounds).
When extracting the organic layer, the sequence of extractions is important: first water (to remove the ammonium salt and the unreacted diethylamine) and then 3M hydrochloric acid (to transfer the lidocaine into the aqueous layer). The sequence of events cannot be changed. Why?
The addition of KOH to the aqueous layer leads to a very strongly basic solution. The product often a yellow oil initially that slowly solidifies to form a waxy solid when placed in an ice-bath. If this does not happen, the mixture has to be stirred vigorously to dissolve the remaining diethyl amine that might interfere with the crystallization.
The product should be collected using a fritted funnel (shown below). Since the solution is very basic at this point, the filter paper slowly but steadily disintegrates during the filtration. The student often times collects a mixture of lidocaine and filter paper fibers afterwards. The funnel should be thoroughly cleaned before being used.
The crude lidocaine is dissolved in a small amout of hexane (~8 mL). If a second layer forms at this point, the layers are separated (which one contains the product?). A small amount of drying agent is added to remove the rest of the water. After decanting the organic layer, the volume is reduced to3-4 mL and the product is allowed to crystallize.
The final product has to be turned in to the TA for evaluation by the instructor by May 4, 2012 at 5 pm. Make sure you label it properly. Otherwise you will not receive any credit!
In some cases, the crude lidocaine does not crystallize. If this is the case, use the following procedure:
1. Extract the crude oil using small portions of petroleum ether (careful!).
2. Add and a spatula of char coal (ask the TA for it) and heat this mixture to a gentle boil for five minutes.
3. Filter the hot suspension using a warm glass funnel with filter paper.
4. Reduce the volume of the solvent to ~5 mL, then allow the solution to cool down to room temperature before placing it in an ice bath.
Finally, do not discard any layer before you isolated the lidocaine and identified it as such by infrared spectrum and melting point. It is not uncommon in this project that the student disposes the wrong layer!