Ketones reductive halogenation

Halocarbons, ketone-alcohol reduction, 84 Halogenation, 4-methylbenzyl chloride [reductive halogenation of aldehyde to benzyl chloride], 124 Hemiacetals, reduction of, 97-99 Hemiaminals, reduction of, 99-100 Hemiketals, reduction of, 97-99 Heptene derivatives, alkene to alkane reductions, disubstituted alkenes, 36-38... 

The carbonyl group in aromatic esters, ketones and acids is transformed into aralkyl bromides or iodides by a one-pot reductive halogenation using LiAlH4/HX reagents (equation 155)988. 

The introduction of tritium into molecules is most commonly achieved by reductive methods, including catalytic reduction by tritium gas, PH2], of olefins, catalytic reductive replacement of halogen (Cl, Br, or I) by H2, and metal pH] hydride reduction of carbonyl compounds, eg, ketones (qv) and some esters, to tritium-labeled alcohols (5). The use of tritium-labeled building blocks, eg, pH] methyl iodide and pH]-acetic anhydride, is an alternative route to the preparation of high specific activity, tritium-labeled compounds. The use of these techniques for the synthesis of radiolabeled receptor ligands, ie, dmgs and dmg analogues, has been described ia detail ia the Hterature (6,7). 

Bromo ketones are commonly employed and are much easier to dehydro-halogenate than chloro ketones, although the latter are not so susceptible to reduction and rearrangement. lodo ketones are generally less accessible and very prone to reduction. 

It is not possible to use zinc for reductive debromination in the presence of (x-halo ketones and for transformations involving these intermediates, sodium iodide has been used. ° In some instances, e.g. 5,6-dihalo-3-ketones, iodide does not always give a completely halogen-free product, and zinc does not give clean debromination. The use of chromous chloride has proved advantageous in such cases and is the reagent of choice for vicinal dichlorides, which are inert to iodide ... 

The success of the halo ketone route depends on the stereo- and regio-selectivity in the halo ketone synthesis, as well as on the stereochemistry of reduction of the bromo ketone. Lithium aluminum hydride or sodium borohydride are commonly used to reduce halo ketones to the /mm-halohydrins. However, carefully controlled reaction conditions or alternate reducing reagents, e.g., lithium borohydride, are often required to avoid reductive elimination of the halogen. 

A thioamide of isonicotinic acid has also shown tuberculostatic activity in the clinic. The additional substitution on the pyridine ring precludes its preparation from simple starting materials. Reaction of ethyl methyl ketone with ethyl oxalate leads to the ester-diketone, 12 (shown as its enol). Condensation of this with cyanoacetamide gives the substituted pyridone, 13, which contains both the ethyl and carboxyl groups in the desired position. The nitrile group is then excised by means of decarboxylative hydrolysis. Treatment of the pyridone (14) with phosphorus oxychloride converts that compound (after exposure to ethanol to take the acid chloride to the ester) to the chloro-pyridine, 15. The halogen is then removed by catalytic reduction (16). The ester at the 4 position is converted to the desired functionality by successive conversion to the amide (17), dehydration to the nitrile (18), and finally addition of hydrogen sulfide. There is thus obtained ethionamide (19)... 

A variation on this theme consists in first displacement of the chlorine in 73 with ethylaminoethanol. Reductive amination of the ketone by means of ammonia in the presence of hydrogen gives the hydroxylated diamine (77). Use of this intermediate to effect displacement of the halogen at the 4 position of 70 affords hydroxychloroquine (78). ... 

---