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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030319Generated: October 25, 2026

Dimethylamine → Tinuvin

https://huagongshe.com/reaction/1030319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTolueneHCID 1140—
Reactant2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxideHCID 14149470—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
ProductTinuvinHCID 6253186.1%

Reaction Steps

33.2 g (0.1 mol) of 2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole-N-oxide, 0.125 g of palladium carbon, 300 ml of a solvent mixture comprising toluene, butanol and water (ratio by volume of 1:1:1) and 5 g 50% dimethylamine were charged into a 500-ml stainless autoclave equipped with an agitator. After the air in the autoclave had been replaced by hydrogen, the pressure of hydrogen was set to 10 kg/cm2. The temperature of the resultant mixture was increased to 50° C. under agitation, and agitation was continued until no more hydrogen gas was absorbed by the mixture. The pressure of hydrogen was always kept at 8 to 10 kg/cm2 during the reaction. After the reaction had been completed, the autoclave was cooled, and the catalyst was filtered off. The most part of solvent was distilled off, and the residual solid was washed with isopropyl alcohol and then dried to obtain 27.2 g of 2-(2'-hydroxy-3'-t-butyl- 5'-methylphenyl)-5-chlorobenzotriazole as a target substance (yield, 86.2%; melting point, 138° to 140° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104992
Source datasetuspto-grants-1992_04
ORD IDord-24723d7b1a7641828cb4c0fff5e4aed4
Source noteuspto-grants-1992_04