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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1706583Erstellt: 24. Oktober 2026

Benzaldehyde → alpha-L-mannopyranose

https://huagongshe.com/de/reaction/1706583

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktBenzoic AcidHCID 243—
EduktWaterHCID 962—
EduktL-mannose phenylhydrazoneHCID 86737045—
LösungsmittelEthanolHCID 702—
Produktalpha-L-mannopyranoseHCID 6971016—

Reaktionsschritte

The hydrazone (20 g.) was then refluxed for 3 hours with a solution containing water (200 ml.), ethanol (40 ml.), benzaldehyde (25 ml.) and benzoic acid (2.5 g.). The solution was cooled and then decanted from benzaldehyde phenylhydrazone, extracted three times with chloroform, decolorized with carbon and concentrated at reduced pressure. The resulting syrup was further evaporated with several portions of absolute ethanol to remove residual water and the resulting syrup (10 g.) was left to crystallize. The crystals were filtered with ethanol to give α-L-mannopyranose, m.p. 125°-126°, [α]D -26.9°→-14.4° (24 hr., c 2.0, water) compared to m.p. 128°-132°, [α]D -14.5° (equilibrium, c 3.4, water).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04207413
Quelldatensatzuspto-grants-1980_06
ORD IDord-53d58275665e4f8ea062e31255bab0d8
Quellennotizuspto-grants-1980_06