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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816743Generated: November 2, 2026

Water → Benzyl 4-(4-hydroxyphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1816743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
Reactantp-(1-Piperazinyl)phenolHCID 92467—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-(4-hydroxyphenyl)piperazine-1-carboxylateHCID 5412373569.4%

Reaction Steps

To a suspension of 1-(4-hydroxyphenyl)piperazine (50 g) and potassium carbonate (46.5 g) in N,N-dimethylformamide (100 ml) was added dropwise benzyl chloroformate (47.86 g) at 0 to 10° C., and stirred for 4 hours at ambient temperature. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with brine and dried, and the solvent was evaporated under reduced pressure. The residue was chromatographed on a column of silica gel eluting with dichloromethane/methyl alcohol (30:1) to give 4-(4-hydroxyphenyl)piperazine-1-carboxylic acid benzyl ester (60.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884868B1
Source datasetuspto-grants-2005_04
ORD IDord-6071c79913c64d0a9b3d1c4286c85368
Source noteuspto-grants-2005_04