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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393844Generated: October 25, 2026

Potassium Carbonate → 2,6-Bis-(1,1-dimethylethyl)-4-{[4-(4-nitrophenyl)-1-piperazinyl]-methyl}-phenol

https://huagongshe.com/reaction/393844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
ReactantPhenol, 4-(bromomethyl)-2,6-bis(1,1-dimethylethyl)-HCID 612973—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2,6-Bis-(1,1-dimethylethyl)-4-{[4-(4-nitrophenyl)-1-piperazinyl]-methyl}-phenolHCID 283866154.3%

Reaction Steps

In a 100 ml flask containing a solution of 2.99 g (10 mmoles) of 2,6-bis-(1,1-dimethylethyl)-4-bromomethylphenol in 30 ml of DMF, 1.38 g (10 mmoles) of potassium carbonate and 2.07 g (10 mmoles) of 1-(4-nitrophenyl)piperazine are added successively. After agitation for two hours at ambient temperature, the reaction medium is diluted with 150 ml of dichloromethane and washed successively with 3×40 ml of water followed by 40 ml of brine. The organic solution is dried over sodium sulphate, filtered and concentrated under reduced pressure. The brown residue obtained is purified on a silica gel column (eluant: petroleum ether (B.p. 40-70° C.)/ethyl acetate: 8/2). After concentration of the pure fractions, 2.31 g (54%) of a brown powder is obtained. Melting point: 177.5-178.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809088B2
Source datasetuspto-grants-2004_10
ORD IDord-c0f2af4779cb4e0b9e7ff8cb0dafc192
Source noteuspto-grants-2004_10