Hydrogen Bromide → 3-Iodophenethyl bromide
Reaction equation
[I:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[CH2:5][CH2:6]O.[BrH:11]>O>[I:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[CH2:5][CH2:6][Br:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3-iodophenethyl alcohol (see Preparation 26) (1.2 g) and 48% aqueous hydrobromic acid (20 ml) was stirred at room temperature for 8 hours, poured into water and extracted into methylene chloride. The organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and water, dried over sodium sulphate and evaporated to give the title compound as a pale brown oil (1.1 g, 73%), which was characterised by its 1H-n.m.r. spectrum.
Workup
- extractionextracted into methylene chloride
- washThe organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and water
- dry with materialdried over sodium sulphate
- customevaporated
Sources & evidence
- ORD record
- ord-75f8aa4f42cf4b778186202485fb0163
- Source dataset
- uspto-grants-1993_07
- Patent number
- US05231104
Reaction notes
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