반응 #9977

ord-b04067277869419fae990d7fe5bba5e8

반응 방정식

Fc1ccc(-c2sc(Br)c(Br)c2-c2ccncc2)cc1
4,5-Dibromo-2-(4-fluorophenyl)-3-(pyridin-4-yl)thiophene
CCCCCC.[Li][CH2]CCC
butyl lithium hexane
O
water
Fc1ccc(-c2scc(Br)c2-c2ccncc2)cc1
title compound
수율 99.7%
Fc1ccc(-c2scc(Br)c2-c2ccncc2)cc1
4-Bromo-2-(4-fluorophenyl)-3-(pyridin-4-yl)thiophene
수율 99.7%

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to warm to room temperature
  2. 2
    기타The reaction mixture was partitioned between a saturated aqueous solution of ammonium chloride and ethyl acetate
  3. 3
    세척The organic layer was washed with water
  4. 4
    건조dried over anhydrous magnesium sulfate
  5. 5
    기타the solvent was removed by distillation under reduced pressure
  6. 6
    세척The residue (solid) was washed with diethyl ether

실험 절차

4,5-Dibromo-2-(4-fluorophenyl)-3-(pyridin-4-yl)thiophene (13.88 g (33.6 mmol), prepared as described in 4)) was dissolved in tetrahydrofuran (140 ml). To the solution was added dropwise at −78° C. a solution of 1.59 M butyl lithium/hexane (23.3 ml, 37 mmol). The resulting mixture was stirred at −78° C. for 15 minutes. At the end of this time, water (24 ml) was added to the reaction mixture and it was allowed to warm to room temperature. The reaction mixture was partitioned between a saturated aqueous solution of ammonium chloride and ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure. The residue (solid) was washed with diethyl ether, to give the title compound (11.20 g) as a pale brown powder (yield quantitative).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091352B2uspto-grants-2006_08