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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032289Generated: October 30, 2026

1-Benzylpiperazine → HCID 15057451, compound

https://huagongshe.com/reaction/1032289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
Reactant2,4-Difluorobenzoyl chlorideHCID 588081—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15057451HCID 1505745187.8%

Reaction Steps

To a stirred and cooled mixture (10° C.) of 64 parts of 1-(phenyl-methyl)piperazine and 360 parts of tetrahydrofuran were added during 20 minutes 32.5 parts of 2,4-difluorobenzoyl chloride. Upon complete addition, stirring was continued until room temperature. The formed salt was filtered off and the filtrate was evaporated in vacuo. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 50 parts (87.8%) of 1-(2,4-difluorobenzoyl)-4-(phenylmethyl)-piperazine as a residue (int. 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957916
Source datasetuspto-grants-1990_09
ORD IDord-f9124086b0284bfd98cd80f8192f4b09
Source noteuspto-grants-1990_09