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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352626Generated: November 2, 2026

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

https://huagongshe.com/reaction/2352626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactantp-(1-Piperazinyl)phenolHCID 92467—
Reactant2-(Chloromethyl)-1,3-benzoxazoleHCID 2061989—
SolventDimethylformamideHCID 6228—
Product1-(4-Hydroxyphenyl)-4-(benzoxazol-2-ylmethyl)piperazineHCID 480662271.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 6.06 g (34 mmol) of 1-(4-hydroxyphenyl)piperazine and 5.36 g (32 mmol) of 2-chloromethylbenzoxazole in 100 ml of absolute DMF was warmed to 80° C., and 737 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 additio of 2.21 g (16 mmol) of K2CO3). The mixture was stirred for a further 3 hours at 80° C., the DMF was substantially removed by distillation in vacuo, and the residue was taken up in 200 ml of ether and 100 ml of water. After separating the phases, the aqueous phase was extracted a further twice with ether. The combined ether extracts were dried, filtered and evaporated in vacuo. The residue was taken up in diisopropyl ether, whereafter crystallization occurred. The crystalline substance was filtered off under suction. 7.10 g (71.7% of theory) of 1-(4-hydroxyphenyl)-4-(benzoxazol-2-ylmethyl)piperazine, melting point 155°-56° C., were obtained,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877878
Source datasetuspto-grants-1989_10
ORD IDord-bdfb4ebcba234d4e83f25f98c59f1a9c
Source noteuspto-grants-1989_10