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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Phenyl-p-phenylenediamine | HCID 7564 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Triphosgene | HCID 94429 | — |
| 반응물 | Benzeneethanamine, 4-nitro-, hydrochloride (1:1) | HCID 458983 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[2-(4-nitrophenyl)-ethyl]-N'-[4-(phenylamino)phenyl]-urea | HCID 22646376 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07186752B2 |
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| 출처 데이터셋 | uspto-grants-2007_03 |
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| ORD ID | ord-241df8e502d2419685b72757de2dc2fb |
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| 출처 메모 | uspto-grants-2007_03 |
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