Journal of Japan Oil Chemists' Society
Online ISSN : 1884-2003
ISSN-L : 0513-398X
Studies on the Syntheses of Mercaptans. VI.
The Effect of Acid Salts on the Reaction of Lauryl Chloride with Sodium Hydrogensulfide in n-Butanol
Takeshi ARAIMotoo KOIKE
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1971 Volume 20 Issue 8 Pages 505-509

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Abstract
The effects of acid salts (NaHCO3, NaHSO4, NaHSO3 and Na2HPO4) on the reaction of lauryl chloride (RCl) with sodium hydrogensulfide (NaSH) in n-butanol were investigated.
Acid salts react with NaSH to generate hydrogensulfide (H2S), which may react with sodium sulfide (Na2S) to yield NaSH. As a whole, the effect of acid salts depends on the following reaction :
Na2S+NaHSO3→Na2SO3+NaSH
The yield of lauryl mercaptan and the amount of distillation residue were nearly the same as the case of addition of H2S presented in the previous paper. The amounts of water and NaSH did not give so much influence on the yield of mercaptan, but the reaction rate decreased with increasing amount of water.
A considerable amount of disulfide (RSSR) formed even in the n-butanol. In the absence of H2S or acid salts, it was presumed that the following reaction occurred :
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