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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248910Generated: October 26, 2026

Trihexylamine → L-Ascorbic Acid

https://huagongshe.com/reaction/2248910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrihexylamineHCID 66022—
ReactantKetogulonsaure-methylesterHCID 54474148—
SolventAcetonitrileHCID 6342—
ProductL-Ascorbic AcidHCID 5467006790.9%

Reaction Conditions

Temperature78 °C

Reaction Steps

26.8 g (128.7 mmol) of ketogulonic acid methyl ester and 125 ml of acetonitrile were added under argon to a 500 ml sulphonation flask provided with a stirrer, thermometer, reflux condenser and 50 ml dropping funnel. Thereupon, the mixture was heated to 78° C. (reflux) while stirring. 34.7 g (100 mol %) of trihexylamine (99.4%) were then added dropwise within 15 minutes from the dropping funnel. The ester passed into solution completely after a reaction period of about 1 hour. After stirring for a total of 21/2 hours at reflux temperature, the orange-brown mixture was added to a rotary perforator gassed with nitrogen. Thereupon, the mixture was extracted continuously with about 500 ml of n-hexane for 20 hours. 1 hour after the beginning of the extraction, ascorbic acid crystallizes out slowly from the acetonitrile phase. After completion of the extraction, the content of the extractor was suction filtered. The yellowish crystals were washed with hexane and acetonitrile and dried overnight in a desiccator. There were obtained 20.6 g of ascorbic acid with a content of 99.5%, corresponding to a yield of 90.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041563
Source datasetuspto-grants-1991_08
ORD IDord-55ef459ff07045299ead303ba57cfa65
Source noteuspto-grants-1991_08