Methanol → 5-Bromomethyl-4-ethoxy-6-trifluoromethylpyrimidine
Reaction equation
[CH2:1]([O:3][C:4]1[C:9]([CH2:10]O)=[C:8]([C:12]([F:15])([F:14])[F:13])[N:7]=[CH:6][N:5]=1)[CH3:2].P(Br)(Br)[Br:17].CO.O>C(OCC)C>[Br:17][CH2:10][C:9]1[C:4]([O:3][CH2:1][CH3:2])=[N:5][CH:6]=[N:7][C:8]=1[C:12]([F:15])([F:14])[F:13]Participants
Conditions
- Temperature
- 0 °C
Procedure
A solution of 3.77 g (17.0 mmoles) of (4-ethoxy-6-trifluoromethylpyrimidin-5-yl)-methanol dissolved in 50 ml of diethyl ether was cooled to 0° C. Thereto was added 2.0 g (7.2 mmoles) of phosphorus tribromide. The mixture was stirred at room temperature for 1 hour. The resulting salt was dissolved using methanol. The resulting mixture was stirred for 1 hour to give rise to a reaction. The reaction mixture was poured into water, followed by extraction with diethyl ether. The resulting organic layer was washed with an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain crude 5-bromomethyl-4-ethoxy-6-trifluoromethylpyrimidine.
Workup
- dissolutionThe resulting salt was dissolved
- stirringThe resulting mixture was stirred for 1 hour
- customto give rise
- customto a reaction
- extractionfollowed by extraction with diethyl ether
- washThe resulting organic layer was washed with an aqueous sodium chloride solution
- dry with materialdried over anhydrous magnesium sulfate
- distillationThe resulting solution was subjected to vacuum distillation
- customto remove the solvent
Sources & evidence
- ORD record
- ord-2f419be3589441148fa331254a205b4d
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07833939B2
Reaction notes
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