You only need to carry out chiral separation and leave D-FB, acidify and recrystallize it, and continue to cool down slowly, without shaking, until the temperature is below zero.
My D is always mixed with some racemization. I think when I use tartaric acid, I don’t pay enough attention to it, but I also extract L. In the end, the total amount of D is always 10~15%. Racemic, but the good news is that when recrystallizing it is always mostly D, and racemic is all around:D
I would like to ask, 5449-12-7 is no longer available for purchase. Is there any alternative that can be substituted? And can it be successfully reduced with NaBH4 with good yield?
There is not enough sodium hydroxide. When producing methylamine gas, the methanol-methylamine solution should be kept at a low temperature to ensure that the methanol absorbs the methylamine gas. Moisture will be produced in the front section. It is recommended to remove the moisture. The...
Is there any new substance that can replace 5449 (old version of sodium salt)?
Can you tell me the CAS or name of the new sodium salt?
I also want to get some and try to use the new version of sodium salt to make P2P
In this method of BOSS, apart from the water problem, is there anything else that will affect the yield?
Why is the yield of methyl free base remaining after evaporating DCM only 50%?
Is there anything I should pay attention to that I haven’t noticed? Please help me~~
@G.Patton
Hello, I would like to ask about what you said about using glycidyl salt instead of sodium salt. How can you tell the difference between these two salts? Is CAS the same?
If you are using L tartaric acid (87-69-4), the solid after mixing is L- and L-tartaric acid. Put the whole bowl in the refrigerator for one day, take it out, add a little methanol and stir, use a filter funnel to separate the solid from the methanol. D-methyl free base can be obtained by adding...