1-Chloro-2,4-Dinitrobenzene → HCID 21875889, compound

HRID 858442Notes

Reaction equation

HRID 858442 reaction equation
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].[NH2:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][OH:23])=[CH:17][CH:16]=1>>[N+:11]([C:3]1[CH:4]=[C:5]([N+:8]([O-:10])=[O:9])[CH:6]=[CH:7][C:2]=1[NH:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][OH:23])=[CH:17][CH:16]=1)([O-:13])=[O:12]

Participants

3

Reactant 2

HCID 61-Chloro-2,4-DinitrobenzeneHCID 669044-Aminophenethyl alcohol

Product 1

HCID 21875889HCID 21875889, compound

Procedure

The title compound was prepared according to the procedure described in step 3 of Example 1 from 2-chloro-1,5-dinitrobenzene and 4-aminophenylethyl alcohol.

Sources & evidence

ORD record
ord-3b8be2f45a8845a9a37d9013d138c924
Source dataset
uspto-grants-2006_12
Patent number
US07148234B2

Reaction notes

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