Lindlar catalyst

A Lindlar catalyst is a heterogeneous catalyst that consists of palladium deposited on calcium carbonate which is then poisoned with various forms of lead or sulphur. It is used for the hydrogenation of alkynes to alkenes (i.e. without further reduction into alkanes) and is named after its inventor Herbert Lindlar.

Synthesis

Lindlar catalyst is commercially available but may also be prepared by the reduction of palladium chloride in a slurry of calcium carbonate (CaCO3) followed by the addition of lead acetate.[1][2] A variety of other "catalyst poisons" have been used, including lead oxide and quinoline. The palladium content of the supported catalyst is usually 5% by weight.

Catalytic properties

The catalyst is used for the hydrogenation of alkynes to alkenes (i.e. without further reduction into alkanes). The lead serves to deactivate the palladium sites, further deactivation of the catalyst with quinoline or 3,6-dithia-1,8-octanediol enhances its selectivity, preventing formation of alkanes, acts as catalyst poison. Thus if a compound contains a double bond as well as a triple bond, only the triple bond is reduced. An example being the reduction of phenylacetylene to styrene.

Alkyne hydrogenation is always stereospecific, occurring via syn addition to give the cis-alkene.[3] An example of commercial use is the organic synthesis of vitamin A which involves an alkyne reduction with the Lindlar catalyst. These catalysts are also used in the synthesis of dihydrovitamin K1.[4]

See also

  • Rosenmund reduction, a reduction using palladium on barium sulphate, poisoned with sulphur compounds.
  • Urushibara Iron, an iron based catalyst used to hydrogenate alkynes to alkenes.

References

  1. ↑ Lindlar, H.; Dubuis, R. (1966). "Palladium Catalyst for Partial Reduction of Acetylenes". Organic Syntheses. doi:10.15227/orgsyn.046.0089. ; Collective Volume, 5, p. 880
  2. ↑ Lindlar, H. (1 February 1952). "Ein neuer Katalysator fur selektive Hydrierungen". Helvetica Chimica Acta. 35 (2): 446–450. doi:10.1002/hlca.19520350205.
  3. ↑ Overman, L. E.; Brown, M. J.; McCann, S. F. (1993). "(Z)-4-(Trimethylsilyl)-3-Buten-1-ol". Organic Syntheses. doi:10.15227/orgsyn.068.0182. ; Collective Volume, 8, p. 609
  4. ↑ Fritz Weber, August Rüttimann "Vitamin K" Ullmann's Encyclopedia Of Industrial Chemistry, 2012, Wiley-VCH, Weinheim. doi:10.1002/14356007.o27_o08
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