Ammonia → HCID 56604232, compound
Reaction equation
[F-].[K+].CN1CCCC1.[F:9][C:10]([Si](C)(C)C)([F:12])[F:11].[Br:17][C:18]1[CH:23]=[C:22](I)[C:21]([F:25])=[CH:20][N:19]=1.N>[Cu](I)I>[Br:17][C:18]1[CH:23]=[C:22]([C:10]([F:12])([F:11])[F:9])[C:21]([F:25])=[CH:20][N:19]=1Participants
Procedure
Copper iodide (1.51 g) and potassium fluoride (0.46 g) were subjected to a reduced pressure (1 Ton) using a vacuum pump, and were heated with a heat gun for 20 minutes while stirring slowly. Under the argon atmosphere, 13 ml of N-methylpyrrolidine and 1.13 g of trifluoromethyltrimethylsilane were added at room temperature, and a temperature was elevated to 50° C. over 20 minutes. After further stirring for 1 hour, 2 g of 2-bromo-5-fluoro-4-iodopyridine was added, and the mixture was stirred for 23 hours. After allowing to cool; the reaction solution was poured into a 12% aqueous ammonia solution, and the resultant solution was extracted with diethyl ether three times, washed with an aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.8 g of 2-bromo-5-fluoro-4-trifluoromethylpyridine.
Workup
- temperaturewere heated with a heat gun for 20 minutes
- stirringAfter further stirring for 1 hour
- stirringthe mixture was stirred for 23 hours
- temperatureto cool
- extractionthe resultant solution was extracted with diethyl ether three times
- washwashed with an aqueous saturated sodium chloride solution
- dry with materialdried with anhydrous magnesium sulfate
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-9b85add863d0475aa0c421b9d230b1d3
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318776B2
Reaction notes
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