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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195248Generated: November 1, 2026

Water → L-ASCORBIC ACID 2-MONOPHOSPHATE TRI-CYCLOHEXYLAMMONIUM SALT

https://huagongshe.com/reaction/1195248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant(+)-5,6-O-Isopropylidene-L-ascorbic acidHCID 54691418—
SolventPyridineHCID 1049—
ProductL-ASCORBIC ACID 2-MONOPHOSPHATE TRI-CYCLOHEXYLAMMONIUM SALTHCID 5467907386%

Reaction Steps

U.S. Pat. No. 4,179,445 discloses another improved method in which 5,6-isopropylidene-L-ascorbic acid, a phosphorus oxyhalide of general formula POX3 (wherein X is a halogen atom) and a specific solvent (a mixed solvent composed of water and a tertiary amine) are mixed with each other and the mixture is kept at pH 13 or higher to react. More particularly, 5,6-isopropylidene-L-ascorbic acid is dissolved in a mixed solvent composed of water and pyridine, and phosphorus oxychloride is added dropwise to the mixture at -10° C. to +10° C. In this case, an aqueous solution of 10M sodium hydroxide is added dropwise to the mixture while stirring in order to carry out the reaction in a higher pH range (e.g., about pH 13). After completion of the reaction, the reaction mixture is cooled to room temperature, treated with a strongly acidic cation exchange resin (H+ -form) for desalting and purification, followed by neutralization with magnesium oxide and removal of the solvent by distillation and dropwise addition of ethanol to the residue to give white powder of magnesium salt of L-ascorbic acid 2-phosphate, which is collected by filtration (yield: 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110951
Source datasetuspto-grants-1992_05
ORD IDord-068f9bc5ff1c45ab83ebbbc69092d056
Source noteuspto-grants-1992_05