Hydrogen Bromide → 1-(2-Bromoethyl)naphthalene
Reaction equation
[BrH:1].O[CH2:3][CH2:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=1>O>[Br:1][CH2:3][CH2:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of hydrobromic acid (50 ml, 46% w/v) and 1-(2-hydroxyethyl)naphthalene (10.0 g, 0.058 mol) was stirred and heated under reflux for 4 h. After cooling, the reaction mixture was diluted with water (150 ml), and the resulting precipitate was extracted with ether (3×150 ml). The ether extracts were combined and dried (MgSO4), when the ether was evaporated under reduced pressure, to afford 1-(2-bromoethyl)naphthalene which was used without further purification.
Workup
- temperatureheated
- temperatureunder reflux for 4 h
- temperatureAfter cooling
- extractionthe resulting precipitate was extracted with ether (3×150 ml)
- dry with materialdried (MgSO4), when the ether
- customwas evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-0ed8f98a63a945f1bb1303c46c1d33fd
- Source dataset
- uspto-grants-1983_11
- Patent number
- US04416895
Reaction notes
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