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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850415Generated: November 2, 2026

N-Methylbenzylamine → N-methyl-1-phenyl-N-[(2,4,6,7-tetramethyl-2,3-dihydro-1-benzofuran-2-yl)methyl]methanamine

https://huagongshe.com/reaction/1850415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbenzylamineHCID 7669—
ReactantPotassium CarbonateHCID 11430—
ReactantDimethylacetamideHCID 31374—
Reactant2-(Iodomethyl)-2,4,6,7-tetramethyl-2,3-dihydro-1-benzofuranHCID 15268305—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-methyl-1-phenyl-N-[(2,4,6,7-tetramethyl-2,3-dihydro-1-benzofuran-2-yl)methyl]methanamineHCID 6676022975%

Reaction Steps

N-methylbenzylamine (766 mg, 3.16 mmol) and potassium carbonate (1.09 g, 7.90 mmol) were added to a solution of DMA (5 mL) containing 2-(iodomethyl)-2,4,6,7-tetramethyl-2,3-dihydro-1-benzofuran (1.00 g, 3.16 mmol) synthesized in Reference Example 126, and the mixture was stirred under heated reflux for 4 hours. The reaction solution was cooled to room temperature, and water and ethyl acetate were added thereto to separate an organic layer. The organic layer was washed with water and saturated saline, and dried using anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was purified by silica gel chromatography (hexane-ethyl acetate 99:1-93:7) to give 730 mg of the title compound (yield: 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957069B2
Source datasetuspto-grants-2015_02
ORD IDord-94c7227b0cfe43b0b6be8e438af43af6
Source noteuspto-grants-2015_02