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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609708Generated: October 31, 2026

Tetrahydrofuran → HCID 178524980, compound

https://huagongshe.com/reaction/1609708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 101711082HCID 101711082—
SolventHydrochloric AcidHCID 313—
ProductHCID 178524980HCID 17852498093%

Reaction Steps

A mixture of 10 g (9.6 mmol) 1,4-O-dicarbotrichloroethoxy-3-O-dicarbotrichloroethoxycaffeoyl quinide is stirred for 5 days at ambient temperature in 65 ml THF and 8 ml concentrated HCl. After separation of the THF and saturation with NaCl, the aqueous phase is extracted with 3×40 ml ethyl acetate. The combined extracts are then washed with brine and dried over sodium sulfate and the solvent is evaporated. Treatment of the residue with a mixture of 1 volume dichloromethane to 10 volumes hexane gives 9.5 g 1,4-O-dicarbotrichloroethoxy-3-O-dicarbotrichloroethoxycaffeoyl quinic acid (yield 93%) in the form of an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401858
Source datasetuspto-grants-1995_03
ORD IDord-8c0a19aeb60349359dcc2d29a0912c12
Source noteuspto-grants-1995_03