Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053662Generated: October 31, 2026

Sodium hydride → HCID 22042659, compound

https://huagongshe.com/reaction/2053662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant4-Bromo-N,2-dimethylanilineHCID 22042599—
SolventDimethylformamideHCID 6228—
ProductHCID 22042659HCID 22042659—

Reaction Steps

To a solution of 2.7 g (13.57 mmol) of N-methyl-4-bromo-2-methylaniline in 20 ml of DMF at room temperature was added 608 mg (15.2 mmol) of NaH and the mixture was stirred at room temperature for 0.5 h. After this time, 2.05 ml (15.1 mmol) of 4-methoxybenzyl chloride was added and the reaction mixture was heated to 60° C. for 12 hours. After this time, the reaction mixture was allowed to cool to room temperature and was quenched by the addition of a saturated aqueous solution of ammonium chloride and extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes:EtOAc, 20:1) to give the title compound. 1H-NMR (CDCl3) δ 2.41 (s, 3H), 2.58 (s, 3H), 3.84 (s, 3H), 3.98 (s, 2H), 6.89-6.94 (m, 3H), 7.26-7.36 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326812B2
Source datasetuspto-grants-2008_02
ORD IDord-623b4bb739804d71acab917da0defb0e
Source noteuspto-grants-2008_02