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Benzonitrile, 4-chloro-3-nitro- → HCID 86752536, 화합물

HRID 618652
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HRID 618652 반응식
Cl[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[N+:10]([O-:12])=[O:11].[CH2:13]([O:15][P:16]([CH:21]([NH2:23])[CH3:22])(=[O:20])[O:17][CH2:18][CH3:19])[CH3:14]>>[CH2:18]([O:17][P:16]([CH:21]([NH:23][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[N+:10]([O-:12])=[O:11])[CH3:22])(=[O:20])[O:15][CH2:13][CH3:14])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 13655Benzonitrile, 4-chloro-3-nitro-HCID 51498581-Diethoxyphosphorylethanamine

생성물 1

HCID 86752536HCID 86752536, 화합물수율 80%

실험 절차

2.77 g (15.24 mmol) of 4-chloro-3-nitrobenzonitrile is stirred with 10.5 g (38 mmol) of 1-aminoethanephosphonic acid diethyl ester for 16 hours at 30° C. The reaction mixture is then chromatographed on silica gel with methylene chloride:ethanol=95:5 as eluant. 3.86 g (80% of theory) of 1-[N-(2-nitro-4-cyanophenyl)amino]ethanephosphonic acid diethyl ester is obtained.

후처리

  1. customThe reaction mixture is then chromatographed on silica gel with methylene chloride

출처 및 근거

ORD 기록
ord-bc3c91ee93824eadbff5ea64fef8e700
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05955461

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