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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030316Generated: October 26, 2026

Dimethylamine → UV-328

https://huagongshe.com/reaction/1030316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant2-(2H-Benzotriazol-2-yl)-4,6-bis(tert-pentyl)phenol N-oxideHCID 11143110—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178503042HCID 178503042—
SolventTolueneHCID 1140—
ProductUV-328HCID 3326396%

Reaction Steps

36.7 g (0.1 mol) of 2-(2'-hydroxy-3',5'-di-t-amylphenyl)benzotriazole-N-oxide, 0.1 g of platinum carbon, 150 ml of a toluene solvent 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 After the air in the flask had been replaced by nitrogen, the resultant mixture was agitated at room temperature.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 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 been 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 96% of 2-(2'-hydroxy-3',5'-di-t-amylphenyl)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 30.5 g of 2-(2'-hydroxy-3',5'-di-t-amylphenyl)benzotriazole (yield, 87%; melting point, 79° to 81° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104992
Source datasetuspto-grants-1992_04
ORD IDord-06067f4cf2014062a6d2c8fe63b28541
Source noteuspto-grants-1992_04