Preparing Alkyl Halides from Alcohols

The most generally useful method for preparing alkyl halides is to make them from alcohols, which themselves can be obtained from carbonyl compounds. Because of the importance of this process, many different methods have been developed to transform alcohols into alkyl halides. The simplest method is to treat the alcohol with HCl, HBr, or HI. This reaction works best with tertiary alcohols, R₃COH. Primary and secondary alcohols react much more slowly and at higher temperatures.

The reaction of HX with a tertiary alcohol is so rapid that it’s often carried out simply by bubbling pure HCl or HBr gas into a cold ether solution of the alcohol. 1-Methylcyclohexanol, for example, is converted into 1-chloro- 1-methylcyclohexane by treatment with HCl.

Primary and secondary alcohols are best converted into alkyl halides by treatment with either thionyl chloride (SOCl₂) or phosphorus tribromide (PBr₃). These reactions, which normally take place readily under mild conditions, are less acidic and less likely to cause acid-catalyzed rearrangements than the HX method.

As the preceding examples indicate, the yields of these SOCl₂ and PBr₃ reactions are generally high and other functional groups such as ethers, carbonyls, and aromatic rings don’t usually interfere. Alkyl fluorides can also be prepared from alcohols. Numerous alternative reagents are used for such reactions, including diethylaminosulfur trifluoride [(CH₃CH₂)₂NSF₃] and HF in pyridine solvent.

مواضيع ذات صلة

Curly arrows are vital for learning organic chemistry

Mechanisms with several steps

Watch out for five-valent carbons

Drawing your own mechanisms with curly arrows

σ bonds as nucleophiles

π bonds as nucleophiles

Charge is conserved in each step of a reaction

Curly arrows show the movement of electrons

Curly arrows represent reaction mechanisms

Identifying an electrophile

Nucleophiles and electrophiles

Orbital overlap is essential for successful reaction