4-Aminophenethyl alcohol → HCID 21875688, compound

HRID 1454655Notes

Reaction equation

HRID 1454655 reaction equation
Cl[C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13].[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][OH:24])=[CH:18][CH:17]=1>>[Cl:8][C:6]1[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][C:3]([N+:12]([O-:14])=[O:13])=[C:2]([CH:7]=1)[NH:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][OH:24])=[CH:18][CH:17]=1

Participants

3

Reactant 2

HCID 669044-Aminophenethyl alcoholHCID 772861,3-Dichloro-4,6-dinitrobenzene

Product 1

HCID 21875688HCID 21875688, compound

Procedure

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

Sources & evidence

ORD record
ord-b69447d5b41945a59de71fafc594a480
Source dataset
uspto-grants-2009_01
Patent number
US07479564B2

Reaction notes

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