Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-keto-L-Gulonic acid | HCID 102424 | — |
| Catalyst | Hexadecyltrimethylammonium chloride | HCID 8154 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | L-Ascorbic Acid | HCID 54670067 | — |
Reaction Steps
A mixture of 2-keto-L-gulonic acid (250 g, content: 89.6%, water: 8.6%) and trimethylcetylammonium chloride (0.275 g) was stirred in toluene (960 ml), and 35% conc. hydrochloric acid (30.0 g) was added. This mixture was stirred at 60° C. for 1 hour, a solution of hydrogen chloride gas (30.0 g) in t-butanol (130 g) was added, and the mixture was stirred at the same temperature for 5 hours. Then, about 1200 g of the solvent was distilled away under reduced pressure while continuously introducing toluene (850 ml). The residue was filtered to give crude crystals of L-ascorbic acid. The crude crystals were dissolved in water. Quantitative analysis of the solution by HPLC showed that the solution contained L-ascorbic acid (50.6 g, yield: 25.0%) and 2-keto-L-gulonic acid (146.8 g, residual ratio: 65.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05637734 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-c973b2c49d9042a09b23b53e2e04ea08 |
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| Source note | uspto-grants-1997_06 |
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