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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477572Generated: October 30, 2026

Sodium hydride → HCID 178518532, compound

https://huagongshe.com/reaction/1477572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
ReactantHCID 178518210HCID 178518210—
SolventDimethylformamideHCID 6228—
ProductHCID 178518532HCID 17851853214%

Reaction Steps

To an N,N-dimethylformamide solution (200 mL) of 1,3,5-triazine-2,4-diol (5.00 g, 44.2 mmol, synthesized according to the method described in Angew. Chem., 74, 354; 1962), sodium hydride (2.12 g, 48.6 mmol, purity 55%) was added at 0° C. and the resultant solution was stirred for 1 hour. To the reaction solution, 4-chlorobenzyl bromide (9.99 g, 48.6 mmol) was added and the resultant solution was stirred at room temperature for 2 hours. After completion of the reaction, saturated ammonium chloride aqueous solution was added thereto, and extraction with ethyl acetate from the resultant mixture was performed. The organic layer was washed with saturated ammonium chloride aqueous solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. To the obtained residue, toluene was added and the solid was collected by filtration, washed with toluene, and dried under reduced pressure to obtain the title compound (1.50 g, yield 14%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-37c2d131e32b4f7f8fb2455cdcac96a4
Source noteuspto-grants-2016_08