2-Bromoethanol → HCID 3051839, compound
Reaction equation
[F:1][C:2]([F:17])([F:16])[C:3]1[CH:4]=[C:5]([N:10]2[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]2)[CH:6]=[CH:7][C:8]=1[F:9].Br[CH2:19][CH2:20][OH:21]>C(O)CCC>[F:17][C:2]([F:16])([F:1])[C:3]1[CH:4]=[C:5]([N:10]2[CH2:11][CH2:12][N:13]([CH2:19][CH2:20][OH:21])[CH2:14][CH2:15]2)[CH:6]=[CH:7][C:8]=1[F:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
10 g (0.04 mole) 4-(3-Trifluoromethyl-4-fluorophenyl)piperazine and 7 g (0.056 mole) 2-bromoethanol are heated under reflux for 4 hours in 60 ml n-butanol. The mixture is left to cool, filtered and then recrystallised from ethanol.
Workup
- waitThe mixture is left
- temperatureto cool
- filtrationfiltered
- customrecrystallised from ethanol
Sources & evidence
- ORD record
- ord-50d9b4073e544fca828a272c53607494
- Source dataset
- uspto-grants-1980_05
- Patent number
- US04203986
Reaction notes
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