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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352625Generated: October 26, 2026

Potassium Carbonate → 1-(4-Hydroxyphenyl)-4-(benzoxazol-2-yl)piperazine

https://huagongshe.com/reaction/2352625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactantp-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
SolventDimethylformamideHCID 6228—
Product1-(4-Hydroxyphenyl)-4-(benzoxazol-2-yl)piperazineHCID 1407416897.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 5.11 g (15 mmol) of 1-(4-hydroxyphenyl)piperazine dihydrobromide, 2.46 g (16 mmol) of 2-chlorobenzoxazole and 2.18 g (15.8 mmol) of powdered K2CO3 in 55 ml of absolute N,N-dimethylformamide was warmed to 85° C., and 345 mg of powdered K2CO3 were added with stirring under a nitrogen atmosphere in each case after 10 minutes, after a further 25 minutes and after a further 60 minutes (total addition of 1.035 g (7.5 mmol) of K2CO3). The mixture was stirred for a further 3 hours at 85° C., the DMF was substantially removed by distillation in an oil-pump vacuum in a rotary evaporator, the crystalline residue was mixed with 50 ml of water, and this mixture was shaken for 15 minutes. The mixture was then filtered under suction and the filter residue was washed with water and dried in vacuo. 4.30 g (97% of theory) of pure 1-(4-hydroxyphenyl)-4-(benzoxazol-2-yl)piperazine, melting point 161°-3° C., were obtained,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877878
Source datasetuspto-grants-1989_10
ORD IDord-34a2e68d44d640428fece298e4783435
Source noteuspto-grants-1989_10