Benzyl Bromide → HCID 20693375, compound
Reaction equation
[C:1]([O:5][C:6](=[O:17])[CH2:7][CH2:8][S:9][C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:18](Br)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[C:1]([O:5][C:6](=[O:17])[CH2:7][CH2:8][S:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:12][CH:11]=1)([CH3:4])([CH3:2])[CH3:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture solution of the compound prepared in Example 1(1) (3.29 g), benzyl bromide (2.3 ml), potassium carbonate (3.58 g) and dimethylformamide (15 ml) was stirred overnight at room temperature. The reaction solution was extracted with ethyl acetate. The extract was washed with water and a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated to give the title compound (2.20 g) having the following physical data.
Workup
- extractionThe reaction solution was extracted with ethyl acetate
- washThe extract was washed with water
- dry with materiala saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-9c7076cea8bb42deafce700fa8a5f7cc
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300514B1
Reaction notes
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