draculic acid69 - 12-8-2018 at 23:09
Just read clorobenzene has difficulty forming a grignard reagent in et2o if it forms at all.apparently it works in thf but this is hard to get for me
and I was under the assumption that clorobenzene just takes longer to initiate but it would still happen in et2o.does anyone have any experience with
clorobenzene in ether or thf ? Would like to know if et2o is a no go and thf is a must or if there are any tips or tricks to forming phenylmagnesium
chloride.
woelen - 12-8-2018 at 23:17
Don't post the same question in multiple forums. One time is enough and you will not get more answers if you post the same thing multiple times. I
close this one, the one in the organic chemistry section is left open for discussion.