It is best to make your own procedure for the equipment and elevation you are in.
Starting temp 90 C. Increase vacuum till you see ethanol coming over. Balance here is fast but not so fast that you have ethanol getting into the vacuum pump.
As the ethanol evaporation dies down you can increase vac or temperature. Whichever lever is easier to pull is what I’d adjust second, in most cases that is vacuum. For example, increase to 100 C and then adjust vacuum up or down to prevent bumping. Bumping is when the stuff in the reactor escapes to the cold trap and/or vacuum.
You’ll reach a point where there is a lot of bubbling but no condensation. That is the decarboxylation and is normal. THCa converting to THC.
Repeat this until you are at 120-130 C and full vacuum. I prefer to go as high as 145 C but this depends on the material and/or farm practices. For example, biomass with high sulfur I’d stop at 120 C and heat it as little as possible for as short a time as possible. Pay attention to your chromatography if you have internal testing or CoAs if not.