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2-Allyl-6-fluorophenol is used as a starting material for the synthesis of organic compounds. It can be obtained by reacting 2-bromo-6-fluorophenol with allyl bromide in the presence of a base. This reaction produces two isomers, 2-(2'-propene)phenol and 2-(2'-isopropenyl)phenol, which are separated by filtration. The yield of this reaction is dependent on the type of solvent used. Hydrocarbon solvents produce higher yields than water or alcohols. This compound can also be synthesized from alkoxybenzenes using peroxide or hydroperoxide.
This molecule has two isomers, cis and trans, that are determined by the orientation of the substituent at carbon atom 3 (see diagram). In both cases, hydrogen atoms at positions 1 and 4 are in the same plane and perpendicular to the other three hydrogens, but they
