반응 #166155

ord-e117e43582cc4668bd745b0af255ca79

반응 방정식

O=C([O-])[O-].[K+].[K+]
potassium carbonate
OB(O)c1ccccc1Br
2-bromophenylboronic acid
Brc1ccc2ccccc2c1
2-bromonaphthalene
N#N
N2
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
Brc1ccccc1-c1ccc2ccccc2c1
title compound
수율 79.6%
Brc1ccccc1-c1ccc2ccccc2c1
2-(2-Bromophenyl)naphthalene
수율 79.6%

반응 조건

온도
85°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a 250-mL round bottom flask equipped with a magnetic stir bar
  2. 2
    기타The solution was sparged with nitrogen for 20 minutes
  3. 3
    온도After cooling to room temperature
  4. 4
    기타the phases were partitioned
  5. 5
    기타the organic layer was collected
  6. 6
    세척The aqueous layer was washed with ethyl acetate (3×30 mL)
  7. 7
    세척the combined organic fractions were washed with brine (60 mL)
  8. 8
    건조dried over sodium sulfate
  9. 9
    여과filtered
  10. 10
    농축concentrated on a rotary evaporator
  11. 11
    기타The crude orange oil was purified by column chromatography on an Isco CombiFlash system (120-g column

실험 절차

To a 250-mL round bottom flask equipped with a magnetic stir bar was added water (25 mL) and 1,2-dimethoxyethane (25 mL). The solution was sparged with nitrogen for 20 minutes, and then potassium carbonate (6.67 g, 48.3 mmol, 3 equiv), 2-bromophenylboronic acid (3.80 g, 18.9 mmol, 0.98 equiv) and 2-bromonaphthalene (4.00 g, 19.3 mmol, 1 equiv) were added. The flask was purged with N2 for 10 minutes before finally adding palladium(II) acetate (87 mg, 0.39 mmol, 0.02 equiv) and triphenylphosphine (405 mg, 1.55 mmol, 0.08 equiv). The reaction mixture was heated to 85° C. under a positive pressure of nitrogen for 7 hours. After cooling to room temperature, the phases were partitioned and the organic layer was collected. The aqueous layer was washed with ethyl acetate (3×30 mL), and the combined organic fractions were washed with brine (60 mL), dried over sodium sulfate, filtered, and concentrated on a rotary evaporator. The crude orange oil was purified by column chromatography on an Isco CombiFlash system (120-g column; gradient: 0.5 column volumes heptane, ramp up to 99:1 heptane:dichloromethane over 0.5 column volumes, hold at 99:1 for 1 column volumes, ramp up to 92:8 heptane:dichloromethane over 7 column volumes, hold at 92:8 for 6 column volumes) to afford the title compound as a colorless oil (4.26 g, 97 area % by HPLC, 78% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.93-7.85 (m, 4H), 7.72 (dd, J=8.0, 1.0 Hz, 1H), 7.57 (dd, J=8.5, 1.7 Hz, 1H), 7.55-7.49 (m, 2H), 7.46-7.38 (m, 2H), 7.28-7.21 (m, 1H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08841487B2uspto-grants-2014_09