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Lipase-assisted generation of 2-methyl-3-furanthiol and 2-furfurylthiol from thioacetates.

Journal of agricultural and food chemistry (2002-06-27)
Rachid Bel Rhlid, Walter Matthey-Doret, Imre Blank, Laurent B Fay, Marcel A Juillerat
RESUMEN

Enzymatic hydrolysis of S-3-(2-methylfuryl) thioacetate and S-2-furfuryl thioacetate using lipase from Candida rugosa produced 2-methyl-3-furanthiol and 2-furfurylthiol, respectively. When reactions were carried out at room temperature and pH 5.8, 2-methyl-3-furanthiol was produced in a optimal yield of 88% after 15 min of reaction, whereas 2-furfurylthiol was obtained in a yield of 80% after 1 h of reaction time. Enzymatic hydrolysis was also performed in n-hexane, n-pentane, and water/propylene glycol mixture. The reaction rates in these media were slower as compared to those in aqueous medium; however, the reaction yields were quite similar. As expected, the stability of the generated 2-methyl-3-furanthiol and 2-furfurylthiol was better in n-hexane, n-pentane, and the water/propylene glycol mixture as compared to that in water or phosphate buffer.

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Sigma-Aldrich
Potassium thioacetate, 98%
Sigma-Aldrich
Thioacetic acid, 96%
Sigma-Aldrich
Furfuryl mercaptan, ≥97%, FG
Sigma-Aldrich
2-Furanmethanethiol, 98%
Sigma-Aldrich
Furfuryl mercaptan, natural, 98%, FG
Sigma-Aldrich
Thioacetic acid, 96%