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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2286818Erstellt: 26. Oktober 2026

Furfural → Formaldehyde

https://huagongshe.com/reaction/2286818

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFurfuralHCID 7362—
Edukt1,4-ButanediolHCID 8064—
EduktBut-2-yne-1,1-diolHCID 18778928—
ProduktFormaldehydeHCID 712—
ProduktAcetyleneHCID 6326—
Produkt2-Butene-1,4-diolHCID 8065—

Reaktionsschritte

Tetrahydrofuran and 1,4-butanediol are both quite useful as organic solvents or as the starting materials for the production of high polymers, and they are manufactured by various processes. For example, it is known that tetrahydrofuran can be produced by the hydrogenation of furan obtained by decarbonylating furfural, or by the dehydrating cyclization of 1,4-butanediol obtainable by hydrogenating either butinediol which can be produced from acetylene and formaldehyde or 2-butene-1,4-diol which can be derived from 1,4-dichlorobutene, or by the hydrogenation of maleic anhydride, or by reacting the acetic ester of 1,4-butanediol with water in the presence of an acidic catalyst. It is also known that 1,4-butanediol can be produced by the hydrogenation of butinediol, or by the hydrolysis of the acetic ester of 1,4-butanediol, or by transesterification reaction of the acetic ester of 1,4-butanediol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04268447
Quelldatensatzuspto-grants-1981_05
ORD IDord-bd684d58cc9343e8954e3f2252aae900
Quellennotizuspto-grants-1981_05