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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030315Generated: November 3, 2026

Dimethylamine → Drometrizole

https://huagongshe.com/reaction/1030315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTolueneHCID 1140—
Reactant2-(2-hydroxy-5-methylphenyl)benztriazole N-oxideHCID 13214646—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventWaterHCID 962—
ProductDrometrizoleHCID 1711367%

Reaction Steps

24.1 g (0.1 mol) of 2-(2'-hydroxy-5'-methylphenyl)benzotriazole-N-oxide, 9.6g of Raney nickel (produced by Kawaken Fine Chemical Co., Ltd.), 150 ml of a solvent mixture comprising toluene and water (ratio by volume, 4:1) and 7 g of 50% dimethylamine were charged into a 500-ml four neck flask. After the air in the flask had been replaced by nitrogen, the resultant mixture was agitated at room temperature. Hydrogen was then supplemented to allow for the amount of hydrogen absorbed by the mixture, which was then subjected to reaction until no more hydrogen was absorbed by it. After the reaction had bee completed, the catalyst was filtered off, and part of the filtrate was subjected to quantitative analysis using gas chromatography (GC). The results revealed a yield of 67% of 2-(2'-hydroxy-5'-methylphenyl)benzotriazole. The solvent was then distilled off from the filtrate, and the residual solid was crystallized using ethanol and then washed with ethanol to obtain 12.4 g of 2-(2'-hydroxy-5'-methylphenyl)benzotriazole (yield, 55%; melting point, 128° to 130° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104992
Source datasetuspto-grants-1992_04
ORD IDord-22fa5b657e044d4a952816d930f32ddf
Source noteuspto-grants-1992_04