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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713493Generated: November 4, 2026

Ammonium Chloride → 2-Benzoyl-1,4-bis(phenylmethyl)piperazine dihydrochloride

https://huagongshe.com/reaction/1713493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1,4-Bis(phenylmethyl)-N-methoxy-N-methyl-2-piperazine carboxamideHCID 23121908—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product2-Benzoyl-1,4-bis(phenylmethyl)piperazine dihydrochlorideHCID 2312183051%

Reaction Steps

1,4-Bis(phenylmethyl)-N-methoxy-N-methyl-2-piperazine carboxamide (2.9 g, 8.1 mmol) was dissolved in tetrahydrofuran (30 mL) under argon atmosphere. A 1.0 M solution of phenylmagnesium bromide in tetrahydrofuran (24 mL, 24 mmol) was added dropwise thereto over 30 minutes with ice cooling. After the mixture was stirred at room temperature for 14 hours, an aqueous saturated ammonium chloride solution (200 mL) was added dropwise thereto with ice cooling, and the resulting mixture was extracted with ethyl acetate (200 ml). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (hexane to hexane:ethyl acetate=2:1). The fractions were collected and concentrated. The residue was dissolved in ethyl acetate, a 4 N hydrogen chloride/ethyl acetate solution (4 mL) was added thereto, and the resulting mixture was stirred at room temperature for 5 minutes. The resulting crystals were collected by filtration and washed with ethyl acetate to obtain the title compound (1.5 g, yield 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795267B2
Source datasetuspto-grants-2010_09
ORD IDord-35d188bd0e4c4051bfe0bbec5725ef8e
Source noteuspto-grants-2010_09