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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850380Generated: November 4, 2026

Dimethylformamide → 4-ethenyl-5-[4-(4-methoxyphenyl)piperazin-1-yl]-2,2,6,7-tetramethyl-1-benzofuran-3(2H)-one

https://huagongshe.com/reaction/1850380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium BicarbonateHCID 516892—
Reactant5-amino-4-ethenyl-2,2,6,7-tetramethyl-1-benzofuran-3(2H)-oneHCID 66759194—
ReactantN,N-bis(2-bromoethyl)-4-methoxyanilineHCID 66759772—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-ethenyl-5-[4-(4-methoxyphenyl)piperazin-1-yl]-2,2,6,7-tetramethyl-1-benzofuran-3(2H)-oneHCID 667602308.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

N,N-bis(2-bromoethyl)-4-methoxyaniline (2.45 g, 7.63 mmol) and sodium hydrogencarbonate (1.25 g, 1.40 mmol) were added to a solution of DMF (36 mL) containing 5-amino-4-ethenyl-2,2,6,7-tetramethyl-1-benzofuran-3(2H)-one (1.47 g, 6.36 mmol) synthesized in Reference Example 22, and the mixture was stirred at 120° C. for 16 hours. After cooled to room temperature, water was added to the mixture, and extraction was performed using ethyl acetate. It was dried using anhydrous magnesium sulfate. After that, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate: 100:0 to 90:10) to give 217 mg of the title compound (yield: 8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957069B2
Source datasetuspto-grants-2015_02
ORD IDord-bee36db59ff64b9d81f88184aa934cdb
Source noteuspto-grants-2015_02