반응 #80456

ord-3e697dd0b9304d75873c4fa489003e9f

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was heated
  2. 2
    온도to reflux under nitrogen
  3. 3
    온도dropwise keeping reflux
  4. 4
    workup.ADDITIONAfter the addition
  5. 5
    온도the mixture was heated
  6. 6
    온도under reflux for 2 h.
  7. 7
    기타under 40° C.
  8. 8
    workup.STIRRINGthe mixture was stirred for 30 min.
  9. 9
    기타the organic layer was separated
  10. 10
    세척washed with 10% sodium thiosulfate solution (50 ml)
  11. 11
    workup.DISTILLATIONby distilled water (100 ml)
  12. 12
    건조The organic layer was then dried over MgSO4
  13. 13
    농축concentrated

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05616596uspto-grants-1997_04