Английская Википедия:Furan-2-ylmethanethiol

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Версия от 16:14, 10 марта 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Use dmy dates|date=December 2021}} {{Chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 457473820 | PIN = (Furan-2-yl)methanethiol | OtherNames = {{Unbulleted list|Furan-2-ylmethanethiol|(2-Furanyl)methylmercaptan|2-Furfurylmercaptan|Furfuryl mercaptan|2-Furfurylthiol|Furfuryl thiol|2-Furylmethanethiol|2-Furylmethyl mercaptan|2-(Mercaptomethyl)furan}} | Im...»)
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Furan-2-ylmethanethiol (2-Furanmethanethiol) is an organic compound containing a furan substituted with a sulfanylmethyl group. It is a clear colourless liquid when pure, but it becomes yellow coloured upon prolonged standing. It possesses a strong odour of roasted coffee and a bitter taste. It is a key component of the aroma of roasted coffee. It has been identified as a trigger molecule for parosmia following COVID-19 infection.[1][2]

Synthesis

Furan-2-ylmethanethiol is easily prepared by reacting furfuryl alcohol with thiourea in hydrochloric acid via an intermediate isothiouronium salt which is hydrolized to the thiol by heating with sodium hydroxide.[3]

Synthesis of furfuryl mercaptane (Furan-2-ylmethanethiol)
Synthesis of furfuryl mercaptane (Furan-2-ylmethanethiol)

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References

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