반응 #80456
ord-3e697dd0b9304d75873c4fa489003e9f
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후처리
- 1온도The mixture was heated
- 2온도to reflux under nitrogen
- 3온도dropwise keeping reflux
- 4workup.ADDITIONAfter the addition
- 5온도the mixture was heated
- 6온도under reflux for 2 h.
- 7기타under 40° C.
- 8workup.STIRRINGthe mixture was stirred for 30 min.
- 9기타the organic layer was separated
- 10세척washed with 10% sodium thiosulfate solution (50 ml)
- 11workup.DISTILLATIONby distilled water (100 ml)
- 12건조The organic layer was then dried over MgSO4
- 13농축concentrated
실험 절차
To a suspension of Mg (3 g, 0.123 mol) in THF (40 ml) was added a small amount of solid I2 (20 mg). The mixture was heated to reflux under nitrogen. To the mixture was then added the 2-bromothiophene solution (5 ml) (19.6 g of 2-bromothiophene in 40 ml of THF). After the iodine color disappeared, to the suspension was added the rest of 2-bromothiophene solution dropwise keeping reflux. After the addition, the mixture was heated under reflux for 2 h., then was cooled to room temperature. To this mixture was added 4-fluorobenzyl iodide (or 4-fluorobenzyl bromide) followed by Li2CuCl4 (5 ml) solution keeping the temperature under 40° C. using a cool water bath. The mixture was stirred at room temperature for 2 h. To the mixture was added sat. NH4Cl solution (100 ml), the mixture was stirred for 30 min., the organic layer was separated and washed with 10% sodium thiosulfate solution (50 ml), followed by distilled water (100 ml). The organic layer was then dried over MgSO4 and concentrated to give 19 g of 2-(4-fluorobenzyl)thiophene as an oil. Purification was achieved by vacuum distillation (110° C., 5 mm Hg).