HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → alpha-L-mannopyranose
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | L-mannose phenylhydrazone | HCID 86737045 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | alpha-L-mannopyranose | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04207413 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-53d58275665e4f8ea062e31255bab0d8 |
| Source note | uspto-grants-1980_06 |