HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium arabinate → D-Arabinonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium arabinate | HCID 86749920 | — |
| Solvent | Water | HCID 962 | — |
| Product | D-Arabinonic acid | HCID 122045 | — |
Reaction Steps
One mole of sodium arabinonate (188 g) in 300 ml of water was acidified on an acid cation exchange resin, giving a solution of arabinonic acid. The arabinonic acid was transformed into the γ-lactone by concentrating in vacuum the aqueous solution to about 200 ml when 300 ml of butanol is added. After a third concentration, the solution is removed from the flask with the aid of 100 ml of butanol and seeded. Crystallization begins at once and a large crop of crystals forms. The crystalline product (115 g) is collected on a filter, washed with butanol and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05563303 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-16d94e34416b45479e241a3f72afdd3d |
| Source note | uspto-grants-1996_10 |