反応式
[CH2:1]([Li])CCC.[F:6][C:7]1[CH:12]=[C:11]([F:13])[C:10]([F:14])=[CH:9][C:8]=1[F:15].CI>CCCCCC.O1CCCC1>[F:6][C:7]1[C:8]([F:15])=[CH:9][C:10]([F:14])=[C:11]([F:13])[C:12]=1[CH3:1]参加物
反応条件
- 温度
- -60 °C
実験手順
A solution of n-butyllithium in hexane (1.6 M, 62.5 ml) was added dropwise to a well stirred solution of 1,2,4,5-tetrafluorobenzene (15.0 g) in dry tetrahydrofuran (150 ml) maintained at a temperature of -60° C. under an atmosphere of dry argon. When the addition was complete the mixture was stirred at -45° C. for 2 hours and then methyl iodide (14.2 g) was added dropwise whilst the temperature was kept at -45° C. After a period of 30 minutes the mixture was allowed to warm to the ambient temperature, poured into distilled water and the mixture extracted with diethyl ether (2×50 ml), and the extracts dried over anhydrous magnesium sulphate. After filtering the solution was concentrated by evaporation of the solvents at atmospheric pressure. The residual oil was distilled and the fraction boiling in the range 115°-122° C. at atmospheric pressure (6.2 g) collected, identified by n.m.r. and gas chromatographic analysis as consisting of ca. 95% of the required 2,3,5,6-tetrafluorotoluene and ca. 5% of 2,3,5,6-tetrafluoro-1,4-xylene.
後処理
- additionWhen the addition
- customwas kept at -45° C
- waitAfter a period of 30 minutes the mixture was allowed
- temperatureto warm to the ambient temperature
- additionpoured
- distillationinto distilled water
- extractionthe mixture extracted with diethyl ether (2×50 ml)
- dry with materialthe extracts dried over anhydrous magnesium sulphate
- filtrationAfter filtering the solution
- concentrationwas concentrated by evaporation of the solvents at atmospheric pressure
- distillationThe residual oil was distilled
- customboiling in the range 115°-122° C. at atmospheric pressure (6.2 g)
- customcollected
出典と根拠
- ORDレコード
- ord-190995229d0445419a832525ac58d9bd
- 出典データセット
- uspto-grants-1983_05
- 特許番号
- US04385070
関連ノート
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