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Ethanol → N-(4-Chlorophenyl)-4-nitroaniline

HRID 986035
ノート
印刷プレビュー

反応式

HRID 986035 の反応式
[CH2:1](O)[CH3:2].[C:4](OCC)(=O)C.[N+:10]([C:13]1[CH:18]=[CH:17][C:16]([NH:19][C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)=[CH:15][CH:14]=1)([O-:12])=[O:11].[OH-].[K+]>C(I)CC.CN(C)C=O.[N+](C1C=CC=CC=1)([O-])=O>[N+:10]([C:13]1[CH:14]=[CH:15][C:16]([N:19]([C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)[CH2:4][CH2:1][CH3:2])=[CH:17][CH:18]=1)([O-:12])=[O:11].[N+:10]([C:13]1[CH:14]=[CH:15][C:16]([NH:19][C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)=[CH:17][CH:18]=1)([O-:12])=[O:11]
参加物実験手順出典と根拠反応ノート

参加物

9

反応物 4

HCID 702EthanolHCID 8857Ethyl AcetateHCID 14797Potassium HydroxideHCID 155617N-(4-Chlorophenyl)-4-nitroaniline

生成物 2

HCID 155617N-(4-Chlorophenyl)-4-nitroanilineHCID 20159089HCID 20159089、化合物

試薬・触媒・溶媒 3

HCID 6228
Dimethylformamide
溶媒
HCID 7416Nitrobenzene溶媒
HCID 336431-Iodopropane溶媒

実験手順

0.90 g of 2,6-difluorobenzoylisocyanate was added to a solution of 1.27 g of 4-[N-(4-chlorophenyl)-N-propylamino]aniline in 15 ml of dry diethylether while stirring at room temperature. After 1.5 hours at room temperature the formed precipitate was sucked off, washed with acetonitrile and diethylether, and dried. The desired product was obtained in a yield of 1.50 g; melting-point 169°-169.5°C. The starting aniline was obtained from the corresponding nitro compound by reduction with hydrogen under the influence of Raney nickel as a catalyst; a mixture of equal parts by volume of ethanol and ethyl acetate was used as a solvent. 1-Nitro-4-[N-(4-chlorophenyl)-N-propylamino]benzene was prepared by an alkylation of 1-nitro-4-(4-chloroanilino) benzene with propyliodide in dimethylformamide as a solvent under the influence of KOH, 1-Nitro-4-(4-chloroanilino) benzene was formed by a coupling at high temperature of p-chlorobenzeneisocyanate and p-nitrophenyl in nitrobenzene as a solvent. In a corresponding manner, in which, if desired, instead of diethylether acetonitrile was used as a solvent for the urea-formation, the following compounds were prepared; the compound numbers correspond with the numbers given before in the specification:

出典と根拠

ORDレコード
ord-da8d252eb08c4a4db8e76206101d21f2
出典データセット
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04710516

反応ノート

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