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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609709Generated: November 1, 2026

Hydrochloric Acid → HCID 178524980, compound

https://huagongshe.com/reaction/1609709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 101711082HCID 101711082—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178524980HCID 178524980—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 12.7 g (12.2 mmol) 1,3-O-dicarbotrichloroethoxy-4-O-dicarbotrichloroethoxycaffeoyl quinide in 870 ml THF is treated for 3 days with 9 ml concentrated HCl. After cooling to 0° C., the reaction mixture is adjusted to pH 2 by addition of solid sodium bicarbonate and is then saturated with NaCl. The organic phase is then separated and the aqueous phase is extracted with 2×20 ml ethyl acetate. After the combined organic phases have been dried over sodium sulfate, the solvents are evaporated. Treatment of the residue with a solvent mixture of THF and hexane in a ratio by volume of 1:20 gives 12.7 g 1,3-O-dicarbotrichloroethoxy- 4-O-dicarbotrichloroethoxycaffeoyl quinic acid in the form of an amorphous white powder (yield 99%) .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401858
Source datasetuspto-grants-1995_03
ORD IDord-ec502971b7a149b8aaa5dd29058f5f42
Source noteuspto-grants-1995_03