돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25044생성일: 2026년 10월 26일

Cyanuric chloride → 4-[[4-Chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]amino]benzonitrile

https://huagongshe.com/reaction/25044

반응식

참여 물질

역할이름HCID투입량
반응물Cyanuric chlorideHCID 7954—
반응물4-AminobenzonitrileHCID 13396—
반응물1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
반응물MagnesiumHCID 5462224—
용매BenzeneHCID 241—
용매Diethyl EtherHCID 3283—
용매1,4-DioxaneHCID 31275—
용매DiisopropylethylamineHCID 81531—
생성물4-[[4-Chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]amino]benzonitrileHCID 486423104.2%

반응 단계

A solution of 2-(bromomethyl)-1,3-dichlorobenzene (about 10% of 0.383 mol) in diethylether (240 ml) was added to magnesium (0.383 mol) in diethylether (240 ml) under argon. Once the reaction started, the remainder of 2-(bromomethyl)-1,3-dichlorobenzene in diethylether was added. The solution was stirred at RT for 2.5 hours and then added via canula to a solution of 2,4,6-trichloro-1,3,5-triazine (0.319 mol) in benzene (480 ml) while keeping the temperature below 15° C. The reaction mixture was stirred for one hour in an ice bath, then for 2 hours at RT. A solution of 4-amino-benzonitrile (0.351 mol) in N,N-diisopropylethylamine (61.0 ml) and 1,4-dioxane (500 ml) was added and the reaction mixture was stirred at RT for 40 hours. The solvent was evaporated. Water and ethylacetate were added. The solution was stirred, then the solid was filtered off, washed with ethylacetate and water, yielding 129.9 g of 4-[[4-chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]-amino]benzonitrile (intermediate 27; mp. 243-244° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858609B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a24fe50e94d9483d807f5b9ce3c92b2c
출처 메모uspto-grants-2005_02