Oh well, a guy I heard about was going the Rp/I2 route with a push pull setup to finally get some honey. He used a 5000ml flat bottom flask and tried to let 178g or Pseudo react. Everything went fine like always, but when phase 2 was ready to kick in, the flask cracked. Luckily this happened not some seconds later, or he might have gotten into big trouble. He took the "always ready for action" wet towels and was able to cool the reaction down, without any further trouble. Since the conversion  did not yet take place, he is wondering about how to continue best from this point?

The reactants are still quite rure. He added about 5ml of water though.  Next smaller flask is 1000ml.

If you seriously can't answer this question yourself get the fuck out.

Lol Damn Sedit. Dont hold back bro...  Hahaha Extreme moderation without prejudice.

No there is alot of prejudice going on right now, I truely hate idiots.

He ran 178g Red Phosphorus and Iodine reaction in more then likely an unworthy container under push pull condition meaning that he used very little water. Not only did he not take the time to do it right and reflux it for 48 hours using a long wet reaction but hes damn lucky he did not just blow his stupid ass up due to PH₃ build up. Then he shows a complete lack of chemical knowledge by asking simple questions like this which is nothing more then a simple workup.

Iv cracked flask into oil baths and managed to recover material even after the highly basic conditions saponified the oil turning it all into a soapy mess. This guy don't even know how to filter acidic water, concentrate his reactants and start the fuck over.

 I say be gone stupid cook! You have destroyed all of our lives with your lack of knowledge. Best way to continue from here is to get a funnel and beer bong the remaining reaction contents then atlest we all win.