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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728323Generated: October 31, 2026

Hydrochloric Acid → HCID 23188865, compound

https://huagongshe.com/reaction/1728323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
Reactant3,4-dihydro-2H-1-benzopyran-2-carboxylic acidHCID 2723665—
Reactant4-Phenyl-4-(4-trifluoromethylphenoxy)piperidineHCID 21268252—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23188865HCID 23188865—

Reaction Steps

A solution of 0.89 g (5.5 mmol) of 1,1-carbonyldiimidazole and 11 ml of dry tetrahydrofuran is added dropwise to a solution of 0.89 g (5.0 mmol) of 3,4-dihydro-2H-1-benzopyran-2-carboxylic acid and 5.5 ml of dry tetrahydrofuran at 20°-25° C. in the course of 1 hour. The reaction solution is then stirred at room temperature for a further 2 hours. A solution of 1.93 g (6.0 mmol) of 4-phenyl-4-(4-trifluoromethyl-phenoxy)-piperidine is then added dropwise at 25° C. in the course of 1 hour. After 18 hours at room temperature, the reaction solution is stirred into a mixture of 220 ml of 5% strength sodium chloride solution, 13 ml of 1 molar hydrochloric acid and 110 ml of toluene for working up. The aqueous phase is extracted once more with 55 ml of toluene. The combined organic phases are then washed with 55 ml each of 0.1 molar hydrochloric acid, followed by 1% strength sodium bicarbonate solution and then water. The organic phase is dried with sodium sulphate and concentrated to dryness.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05326771
Source datasetuspto-grants-1994_07
ORD IDord-9be23452aae0441c8e7d7a7ecf134392
Source noteuspto-grants-1994_07