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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1272569Erstellt: 23. Oktober 2026

Hydrochloric Acid → 5-Formylfuran-2-boronic acid

https://huagongshe.com/de/reaction/1272569

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTrimethyl borateHCID 8470—
EduktChlorocyclohexaneHCID 10952—
EduktFurfural diethyl acetalHCID 83553—
EduktLithiumHCID 3028194—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelCyclohexaneHCID 8078—
Produkt5-Formylfuran-2-boronic acidHCID 273435577%

Reaktionsbedingungen

Temperatur-65 °C

Reaktionsschritte

A mixture of 20.88 g of chlorocyclohexane (0.176 mol) and 27.2 g of furfural diethyl acetal (0.16 mol) is added dropwise to a suspension of 2.35 g of lithium granules (0.34 mol) in 300 g of THF at −65° C., with an addition time of 2 hours being selected. After a conversion of the chlorocyclohexane of >97% determined by GC (total of 10 h), 18.3 g of trimethyl borate (0.176 mol) are added dropwise at the same temperature over a period of 30 minutes. After stirring for another 30 minutes at −65° C., the reaction mixture is poured into 120 g of water, the pH is adjusted to 6.3 by means of 37% HCl, and THF and cyclohexane are distilled off at a maximum of 35° C. under reduced pressure. The pH is subsequently adjusted to 1.5, the mixture is stirred until all the product has precipitated and the product is filtered off. After washing with a little cold water and a little cold acetone and drying, 17.2 g of 5-formyl-2-furanboronic acid (0.123 mol, 77%) are obtained in the form of a fine beige powders, HPLC purity >99% a/a.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07208614B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-f5a5e39256e84d8ebd11ba0120058d4c
Quellennotizuspto-grants-2007_04