1,2-Dibromoethane → HCID 18548202, compound
Reaction equation
[Mg].BrCCBr.[CH2:6]([O:8][CH:9]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17]Br)[CH3:10])[CH3:7].Br[CH2:20][C:21]([Br:23])=[CH2:22]>C1COCC1>[CH2:6]([O:8][CH:9]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:22][C:21]([Br:23])=[CH2:20])[CH3:10])[CH3:7]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 45 °C
Procedure
A slurry of 5.6 g of magnesium turnings (230 mmol) in 100 ml of THF was treated with a small amount of 1,2-dibromoethane. 1-(1-Ethoxyethoxy)-6-bromohexane (38.5 g, 152 mmol) was fed slowly to the reaction mixture, maintaining the temperature at 40-50° C. At the end of the addition the reaction mixture was held 20 minutes, then transferred by cannula to solution of 33.4 9 (167 mmol) of 1,2-dibromoprop-2-ene in 25 ml of THF at 0C. The reaction mixture was stirred at 0° C. for 15 minutes, then stirred at room temperature for 15 minutes, then quenched with water. The reaction mixture was transferred into a separatory funnel. A small amount of 1 N HCl was added, the phases were separated, the ether phase was washed with water and brine, then dried over magnesium sulfate, filtered, and stripped to give 33.63 g of a yellow liquid which was used without further purification.
Workup
- additionAt the end of the addition the reaction mixture
- stirringstirred at room temperature for 15 minutes
- customquenched with water
- customThe reaction mixture was transferred into a separatory funnel
- additionA small amount of 1 N HCl was added
- customthe phases were separated
- washthe ether phase was washed with water and brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
Sources & evidence
- ORD record
- ord-fc107c9a23ca43098e1f535872d8c881
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06365549B2
Reaction notes
Loading…