反应 #80442

ord-e27ba103370d43dd91c69944a80b85e4

反应方程式

[Cl-].[NH4+]
ammonium chloride
c1ccoc1
furan
Fc1ccc(CBr)cc1
4-fluorobenzyl bromide
[Li][CH2]CCC
n-butyllithium
CCCCCC
hexane
Fc1ccc(Cc2ccco2)cc1
2-(4-fluorophenylmethyl)furan
收率 81.2%

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他transferred by cannula to a stirred -78° C.
  2. 2
    workup.WAITThe transfer was made under nitrogen over a period of 30-40 minutes
  3. 3
    workup.STIRRINGThe reaction mixture was stirred at ambient temperature overnight
  4. 4
    萃取the mixture extracted with ether
  5. 5
    干燥The ether layer was dried (MgSO4)
  6. 6
    浓缩concentrated in vacuo
  7. 7
    workup.DISTILLATIONthe residue distilled at reduced pressure

实验过程

To a 0° C. solution of furan (13.6 g, 0.20 mol) in a mixture of anhydrous ether (230 mL) and anhydrous THF (70 mL) under nitrogen was added a 2.5M solution of n-butyllithium in hexane (54.0 mL, 0.134 mol). The mixture was stirred at 0° C. for 1.5 hours and then transferred by cannula to a stirred -78° C. solution of 4-fluorobenzyl bromide (23.6 g, 0.125 mol) and tetrakis-(triphenylphosphine)palladium (O) (1.25 g, 0.001 mol) in anhydrous THF (200 mL). The transfer was made under nitrogen over a period of 30-40 minutes. The reaction mixture was stirred at ambient temperature overnight, saturated aqueous solution of ammonium chloride was added and the mixture extracted with ether. The ether layer was dried (MgSO4), concentrated in vacuo and the residue distilled at reduced pressure to give 2-(4-fluorophenylmethyl)furan as a colorless oil (17.89 g, 81% ). b.p. 57°-62° C. at 0.5-0.7 mm-Hg.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05616596uspto-grants-1997_04