Hydrochloric Acid → 2-Nitro-1-[3-(trifluoromethyl)phenyl]ethanamine hydrochloride
Reaction equation
[N+:1]([CH2:4][CH:5]([NH:16]C(=O)OC(C)(C)C)[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([C:12]([F:15])([F:14])[F:13])[CH:7]=1)([O-:3])=[O:2].[ClH:24]>O1CCOCC1>[ClH:24].[N+:1]([CH2:4][CH:5]([C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([C:12]([F:13])([F:14])[F:15])[CH:7]=1)[NH2:16])([O-:3])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Of the compound from Example 12A, 340 mg (1.02 mmol) were admixed at RT with 6.8 ml of a 4N solution of hydrogen chloride in dioxane, and stirred for 1 h. The reaction mixture was concentrated under reduced pressure and dried in an HV. This gave 274 mg (99% of theory) of the title compound.
Workup
- concentrationThe reaction mixture was concentrated under reduced pressure
- customdried in an HV
Sources & evidence
- ORD record
- ord-9f140f45327940efaf8114ff642eb124
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08202895B2
Reaction notes
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