
doi: 10.1246/bcsj.29.265
Abstract 1. Hydrogen sulphide cooking of α-guaiacyl propanol (VI) gave bis(1-(4-hydroxy-3-methoxyphenyl)-1-propyl) monosulphide (VIII) and disulphide (VII). 2. Vanillyl monosulphide was decomposed with alkali at 130°. Vanillin, vanillyl alcohol and the secondary products from vanillyl alcohol were identified. 3. The mechanism of the kraft cooking process was discussed and a new mechanism was proposed.
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