반응 #171527

ord-bbfd30650a9148d39f28af8f5a2880c9

반응 방정식

Brc1ccc(-c2ccccc2)cc1
4-Bromobiphenyl
C#CCCCO
4-pentyn-1-ol
OCCCC#Cc1ccc(-c2ccccc2)cc1
title compound
수율 75.0%
OCCCC#Cc1ccc(-c2ccccc2)cc1
5-(1,1′-biphenyl-4-yl)-pent-4-yn-1-ol
수율 75.0%

반응 조건

온도
65°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was cooled to room temperature
  2. 2
    여과filtered through a celite pad
  3. 3
    세척rinsed with ethylacetate
  4. 4
    기타The combined filtrate was evaporated to dryness under reduced pressure
  5. 5
    기타The resulting residue was purified by column chromatography (hexanes:ethylacetate 3:2)

실험 절차

4-Bromobiphenyl (10.28 g, 44.10 mmol), 4-pentyn-1-ol (4.45 g, 52.92 mmol), and bis(triphenylphosphine)palladium(II) dichloride (310 mg, 0.44 mmol) were stirred in triethylamine (100 mL) under nitrogen for 5 min. Copper(I) iodide (42 mg, 0.22 mmol) was added, and the mixture was stirred for 4 hrs at 65° C. The mixture was cooled to room temperature and filtered through a celite pad, rinsed with ethylacetate. The combined filtrate was evaporated to dryness under reduced pressure. The resulting residue was purified by column chromatography (hexanes:ethylacetate 3:2) to afford 7.78 g of the title compound. Yield: 75%. 1H NMR (300 MHz, CDCl3) δ 1.88 (m, 2H), 2.57 (t, J=6.9 Hz, 2H), 3.84 (t, J=6.0 Hz, 2H), 7.32-7.60 (m, 9H) ppm; 13C NMR (75 MHz, CDCl3) δ 16.4, 31.7, 62.1, 81.2, 90.2, 122.8, 127.0, 127.1, 127.6, 128.9, 132.0, 140.1 ppm.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08846937B2uspto-grants-2014_09