Sorry if this is old news, but I couldn't find it anywhere so I figured I'd share.
After doing a bunch of vinegar lime A/B extractions, I found myself getting a little frustrated with freeze precipitation (patience is a virtue I could probably use some work on).
Not wanting to stank up my house with naphtha fumes via evaporation with a fan I decided to try distilling the naphtha off until a very small volume of liquid remained, then evaporating that by fan. I have had great success with this method, and It is much faster than freeze precipitation. You will end up with goo, but you can always recrystalize it, and more easily so due to the small volume of liquid, though I assure you the goo is quite active as is.
I'm using a Vigreux column and water cooled Liebig condenser, but I'm sure plenty of the resourceful folks on here can make due with less.
Super quick extraction, no naphtha fumes going into the air, and the solvent is easily recycled as it condenses right back into the liquid phase.
Are there any disadvantages to this method that I might be unaware of? It seems to have been working pretty well for me, though I am getting a bit tired of scraping goo off of my evaporation dish.