돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456857생성일: 2026년 10월 25일

N-Phenyl-p-phenylenediamine → N-[2-(4-nitrophenyl)-ethyl]-N'-[4-(phenylamino)phenyl]-urea

https://huagongshe.com/reaction/456857

반응식

참여 물질

역할이름HCID투입량
반응물N-Phenyl-p-phenylenediamineHCID 7564—
반응물DiisopropylethylamineHCID 81531—
반응물TriphosgeneHCID 94429—
반응물Benzeneethanamine, 4-nitro-, hydrochloride (1:1)HCID 458983—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-[2-(4-nitrophenyl)-ethyl]-N'-[4-(phenylamino)phenyl]-ureaHCID 2264637640%

반응 단계

0.5 g (1.7 mmol) of triphosgene is dissolved in 8 ml of dichloromethane in a 100 ml flask, under argon. Using a motorized syringe, a solution of 0.92 g (5 mmol) of 4-aminodiphenylamine and 1.44 ml (8.2 mmol) of diisopropylethylamine in 15 ml of dichloromethane is added over one hour. Five minutes after the addition is finished, 1.01 g (5 mmol) of 4-nitrophenethylamine hydrochloride followed by a solution of 1.44 ml (8.2 mmol) of diisopropylethylamine in 10 ml of dichloromethane are added in a single portion. After agitation for two hours at 20° C., the reaction mixture is diluted with 50 ml of dichloromethane and 20 ml of water. The organic phase is decanted and rewashed with 20 ml of water. After drying over, MgSO4 and filtration, the organic solution is partially concentrated under vacuum. The precipitate formed is collected by filtration and rinsed with dichloromethane. A yellow solid is obtained with a yield of 40%. Melting point: 204–205° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186752B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-241df8e502d2419685b72757de2dc2fb
출처 메모uspto-grants-2007_03