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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706583Generated: October 26, 2026

Benzaldehyde → alpha-L-mannopyranose

https://huagongshe.com/reaction/1706583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBenzoic AcidHCID 243—
ReactantWaterHCID 962—
ReactantL-mannose phenylhydrazoneHCID 86737045—
SolventEthanolHCID 702—
Productalpha-L-mannopyranoseHCID 6971016—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207413
Source datasetuspto-grants-1980_06
ORD IDord-53d58275665e4f8ea062e31255bab0d8
Source noteuspto-grants-1980_06