Hydrogen Bromide → HCID 67283800, compound
Reaction equation
S([N:11]1[CH2:16][CH2:15][N:14]([CH2:17][C:18]([F:21])([F:20])[F:19])[CH2:13][CH2:12]1)(C1C=CC(C)=CC=1)(=O)=O.[BrH:22].C(O)(=O)C.Br>C1(C)C=CC=CC=1>[BrH:22].[BrH:22].[F:21][C:18]([F:19])([F:20])[CH2:17][N:14]1[CH2:13][CH2:12][NH:11][CH2:16][CH2:15]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
A suspension of 1-tosyl-4-(2,2,2-trifluoroethyl)piperazine (700 mg, 2.2 mmol) in a 30% HBr/acetic acid solution was stirred at 90° C. for 90 minutes. Toluene was added to the suspension. An orange solid was filtered off and washed with diethyl ether to afford the desired compound (400 mg, 55% yield) as a bis HBr salt.
Workup
- filtrationAn orange solid was filtered off
- washwashed with diethyl ether
Sources & evidence
- ORD record
- ord-5f611412e4834a08b12e9c9c8019c399
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08455507B2
Reaction notes
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