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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942557Generated: November 2, 2026

Benzoic Acid → HCID 67330689, compound

https://huagongshe.com/reaction/1942557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 67330916HCID 67330916—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 67330689HCID 6733068945.6%

Reaction Steps

To a solution of tert-butyl (rac.)-(3R,4R)-3-(ethylamino)-4-(3-hydroxyphenyl)piperidine-1-carboxylate (1.76 g) in methylene chloride (16 ml) were added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.37 g), N,N-dimethylaminopyridine (872 mg), triethylamine (995 μl), and benzoic acid (610 mg), and the mixture was stirred at room temperature for one hour. To the reaction mixture was added a saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous ammonium chloride solution, a saturated aqueous sodium hydrogen carbonate solution, and a saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (the developing solvent: hexane/ethyl acetate=1/1) to give the title compound (968 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389511B2
Source datasetuspto-grants-2013_03
ORD IDord-3932d3c2e4954708bebd7192254f1986
Source noteuspto-grants-2013_03