HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609709Generated: November 1, 2026
Hydrochloric Acid → HCID 178524980, compound
https://huagongshe.com/reaction/1609709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 101711082 | HCID 101711082 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178524980 | HCID 178524980 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401858 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-ec502971b7a149b8aaa5dd29058f5f42 |
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| Source note | uspto-grants-1995_03 |
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