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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791002Generated: November 1, 2026

Sodium hydride → HCID 22042659, compound

https://huagongshe.com/reaction/1791002

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), 7.29–7.36 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071358B2
Source datasetuspto-grants-2006_07
ORD IDord-c7de15a5b80d4d3ca1aea6c4a4e5da0b
Source noteuspto-grants-2006_07