돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1030319생성일: 2026년 10월 27일

Dimethylamine → Tinuvin

https://huagongshe.com/reaction/1030319

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물TolueneHCID 1140—
반응물2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxideHCID 14149470—
반응물HCID 178418361HCID 178418361—
촉매HCID 178418390HCID 178418390—
용매1-ButanolHCID 263—
용매WaterHCID 962—
생성물TinuvinHCID 6253186.1%

반응 단계

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 After the air in the autoclave had been replaced by hydrogen, the pressure of hydrogen was set to 10 kg/cm2.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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05104992
출처 데이터셋uspto-grants-1992_04
ORD IDord-24723d7b1a7641828cb4c0fff5e4aed4
출처 메모uspto-grants-1992_04