4-Chloro-2-(2,4-dinitroanilino)phenol → 2-(2-Nitroanilino)phenol

Reaction equation

Cl[C:2]1[CH:3]=[CH:4][C:5]([OH:21])=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([N+]([O-])=O)=[CH:11][C:10]=2[N+:18]([O-:20])=[O:19])[CH:7]=1.[N+](C1C=C([N+]([O-])=O)C=CC=1N1C2C=C(Cl)C=CC=2OC1=O)([O-])=O>>[OH:21][C:5]1[CH:4]=[CH:3][CH:2]=[CH:7][C:6]=1[NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[N+:18]([O-:20])=[O:19]

Participants

Reactant 2

HCID 53601534-Chloro-2-(2,4-dinitroanilino)phenol

HCID 19771087HCID 19771087, compound

Product 1

HCID 142248152-(2-Nitroanilino)phenol

Procedure

N-(5-chloro-2-hydroxyphenyl)-2,4-dinitroaniline from N-(2,4-dinitrophenyl)-5-chloro-2-benzoxazolinone. The product was used without further purification.

Workup

customThe product was used without further purification

Sources & evidence

ORD record: ord-c3ee6d19a4444ac9b43db64553b2d774
Source dataset: uspto-grants-1993_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05200422

Reaction notes

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