4-Aminophenethyl alcohol → HCID 21876115, compound

HRID 2077683Notes

Reaction equation

HRID 2077683 reaction equation
F[C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[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>>[CH3:8][C:6]1[CH:5]=[CH:4][C:3]([N+:9]([O-:11])=[O:10])=[C:2]([CH:7]=1)[NH:12][C:13]1[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][OH:21])=[CH:15][CH:14]=1

Participants

3

Reactant 2

HCID 669044-Aminophenethyl alcoholHCID 67966Benzene, 2-fluoro-4-methyl-1-nitro-

Product 1

HCID 21876115HCID 21876115, compound

Procedure

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

Sources & evidence

ORD record
ord-fb8fb9542e3b4945ae1a3aa851ee2947
Source dataset
uspto-grants-2011_04
Patent number
US07928119B2

Reaction notes

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