wolfx
(Hive Bee) 11-10-03 18:07 No 470059 |
Wacker oxidation workup doubts | |||||||
I would like if possible to understand better the reasons for the several steps used after the Wacker oxidation. I would expose what I have been thinking about it, please correct me if and wherever I am wrong. Filtering removes the PdCl2 catalyst. Pouring the reaction contents in the 10 % HCl dilutes the DMF and creates a two phase solution, water + DMF on top, ketone on the bottom. Next we extract the watery layer with DCM and combine. One question, why the HCl ? If using only H2O, same effect ? Now, what about hydroquinone and p-benzo ? I think we have some of each mixed in with ketone, DCM and black tar. Looks like both p-benzo and hydroquinone do not react with acids, it this correct ? I know hydroquinone is supposed to be removed with the NaOH washes. Same for any remaining p-benzo ? Does p-benzo reacts with NaOH as well ? What are the end products of the p-benzo + NaOH, hydroquinone + NaOH reactions ? One last question, I have seen several times this asked, never answered : What is the reason for the sodium bicarbonate and brine washes ? |
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scram (Hive Bee) 11-10-03 22:45 No 470122 |
"Filtering removes the PdCl2 ... | |||||||
"Filtering removes the PdCl2 catalyst." I wish you good luck trying that! Unless you do the filetering after the addition of NaOH. |
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Rhodium (Chief Bee) 11-11-03 01:05 No 470142 |
UTFSE | |||||||
One question, why the HCl ? If using only H2O, same effect ? Decomposing intermediates into the desired end product. Follow the instructions. What is the reason for the sodium bicarbonate and brine washes Removing undesired contaminants (DMF, Salts) and pre-drying the solution. Post 394075 (pHarmacist: "Washing with brine", Newbee Forum) |
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