4-Aminophenethyl alcohol → HCID 21876163, compound

HRID 858428Notes

Reaction equation

HRID 858428 reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[NH2:12][C:13]1[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][OH:21])=[CH:15][CH:14]=1>>[F:8][C:5]1[CH:6]=[CH:7][C:2]([NH:12][C:13]2[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][OH:21])=[CH:15][CH:14]=2)=[C:3]([N+:9]([O-:11])=[O:10])[CH:4]=1

Participants

3

Reactant 2

HCID 669044-Aminophenethyl alcoholHCID 677672,5-Difluoronitrobenzene

Product 1

HCID 21876163HCID 21876163, compound

Procedure

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

Sources & evidence

ORD record
ord-a6808d97578945f08a462da656fefff2
Source dataset
uspto-grants-2006_12
Patent number
US07148234B2

Reaction notes

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