Hydrogen Bromide → HCID 20096775, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:10]2[CH2:15][CH2:14][CH:13]([CH2:16][CH2:17]O)[CH2:12][CH2:11]2)[CH:5]=[C:6]([F:9])[C:7]=1[F:8].[BrH:19]>O>[F:1][C:2]1[CH:3]=[C:4]([CH:10]2[CH2:15][CH2:14][CH:13]([CH2:16][CH2:17][Br:19])[CH2:12][CH2:11]2)[CH:5]=[C:6]([F:9])[C:7]=1[F:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4-(3',4',5'-Trifluorophenyl)-1-(2'-hydroxyethyl)cyclohexane (10.4 g) was added to an aqueous solution of 47% HBr (15 ml), followed by stirring the mixture under reflux for 2 hours, adding the reaction solution to water (50 ml), extracting with ethyl acetate (100 ml), washing the organic layer with water, drying over anhydrous MgSO4, and concentrating the solvent under reduced pressure, to obtain 4-(3',4',5'-trifluorophenyl)-1 -(2'-bromoethyl)cyclohexane (10.4g).
Workup
- temperatureunder reflux for 2 hours
- extractionextracting with ethyl acetate (100 ml)
- washwashing the organic layer with water
- dry with materialdrying over anhydrous MgSO4
- concentrationconcentrating the solvent under reduced pressure
Sources & evidence
- ORD record
- ord-3c920d3407ac4374886efeb8579b60ef
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05382379
Reaction notes
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