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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2397603생성일: 2026년 10월 27일

Sodium Hydroxide → 3,3',5,5'-Tetramethylbenzidine

https://huagongshe.com/reaction/2397603

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물4-Bromo-2,6-xylidineHCID 90549—
반응물Sodium FormateHCID 2723810—
촉매Hexadecyltrimethylammonium BromideHCID 5974—
촉매PalladiumHCID 23938—
용매WaterHCID 962—
생성물3,3',5,5'-TetramethylbenzidineHCID 4120663.3%

반응 단계

4-Bromo-2,6-dimethylaniline (24.0 parts), 3% palladium on charcoal (50% paste; 2.0 parts), cetyltrimethylammonium bromide (4.0 parts), sodium hydroxide liquor (32%; 13.5 parts), sodium formate (6.8 parts) in water (60 parts) are stirred at the boil under reflux for 3 hours. Sodium formate (6.8 parts is then added and the mixture boiled for 3 hours when a further charge of sodium formate (6.8 parts) is made. The reaction mixture is then held at the boil under reflux for a further 23 hours. The mixture is then steam distilled and from the distillate 2.2 parts (18.2%) of 2,6-dimethylaniline is recovered by extraction with ether. The reaction mixture after steam distillation is cooled to room temperature and then filtered. The residue is extracted continuously with methanol (60 parts) for 5 hours and then the extract cooled. The colourless crystalline precipitate is filtered off and dried to give 7.7 parts (63.3%) of 3,3',5,5'-tetramethyl benzidine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04022795
출처 데이터셋uspto-grants-1977_05
ORD IDord-e442844c76fd4e4d833b347290a3306d
출처 메모uspto-grants-1977_05