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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683373Generated: November 1, 2026

Hydrochloric Acid → L-Ascorbic Acid

https://huagongshe.com/reaction/1683373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant2-keto-L-Gulonic acidHCID 102424—
CatalystHexadecyltrimethylammonium chlorideHCID 8154—
SolventDiisopropyl EtherHCID 7914—
ProductL-Ascorbic AcidHCID 54670067—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-keto-L-gulonic acid (125 g, 0.584 mol, content: 90.7%, water: 8.5%) and trimethylcetylammonium chloride (0.084 g) was stirred in diisopropyl ether (500 ml), and 36% conc. hydrochloric acid (18.0 g) was added. At this time, the amount of water in the reaction system was calculated as 2.1 mol per mol of 2-keto-L-gulonic acid. This mixture was stirred at 60° C. for 1 hour, a solution of hydrogen chloride gas (17.2 g) in diisopropyl ether (88 g) was added, and the mixture was stirred at the same temperature for 5 hours. Then, about 900 g of the solvent was distilled away under reduced pressure while continuously introducing diisopropyl ether (1000 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 (95.8 g, yield: 93.1%) and 2-keto-L-gulonic acid (0.9 g, residual ratio: 0.8%). Quantitative analysis of diisopropyl ether in the distillate and filtrate showed that the recovery ratio was not less than 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637734
Source datasetuspto-grants-1997_06
ORD IDord-d692cac574a54aab95de38fdfec7affb
Source noteuspto-grants-1997_06