Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850432Generated: November 1, 2026

4-Bromo-1-methoxy-2-methylbenzene → HCID 59485110, compound

https://huagongshe.com/reaction/1850432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1-methoxy-2-methylbenzeneHCID 608315—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant1-(2,4,6,7-Tetramethyl-2,3-dihydro-1-benzofuran-5-yl)piperazineHCID 66759810—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 59485110HCID 5948511019.5%

Reaction Steps

To the toluene (3.1 mL) solution of 1-(2,4,6,7-tetramethyl-2,3-dihydro-1-benzofuran-5-yl)piperazine (400 mg, 1.54 mmol) synthesized in Reference example 56, 4-bromo-1-methoxy-2-methylbenzene (464 mg, 2.31 mmol), palladium acetate (17 mg, 0.077 mmol), BINAP (143 mg, 0.231 mmol) and sodium tert-butoxide (296 mg, 3.08 mmol) were added and irradiated with microwave. The mixture was reacted for 15 minutes at 150° C. To the mixture solution, water was added and extracted with ethyl acetate. The extract solution was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate 85:15). The resulting solid was recrystallized from ethanol to obtain the title compound 114 mg (yield 19%). Melting point was 141 to 142° C. (ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957069B2
Source datasetuspto-grants-2015_02
ORD IDord-7f791769dc5a452eb8a7f903320fc9ac
Source noteuspto-grants-2015_02