Benzene, 1-bromo-3-iodo- → ((3-Bromophenyl)ethynyl)trimethylsilane

HRID 2400026Notes

Reaction equation

HRID 2400026 reaction equation
[Br:1][C:2]1[CH:3]=[C:4](I)[CH:5]=[CH:6][CH:7]=1.[CH3:9][Si:10]([C:13]#[CH:14])([CH3:12])[CH3:11]>C(NC(C)C)(C)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Cu]I>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:14]#[C:13][Si:10]([CH3:12])([CH3:11])[CH3:9])[CH:3]=1

Participants

6

Procedure

To a solution of m-bromoiodobenzene (25.0 g. 881.1 mmol) in diisopropylamine (500 ml), there were added bis(triphenylphosphine)palladium dichloride (1.24 g. 1.80 mmol) and copper (I) iodide (1.24 g, 2.03 mmol). The solution was degassed via a rapid stream of argon, and trimethylsilylacetylene (9.51 g, 97.0 mmol) was added over a period of 15 min. The reaction mixture was stirred at room temperature until G.C. analysis indicated the disappearance of starting material (2 h). The reaction mixture was cooled to room temperature and filtered to remove salts. The filtrate was concentrated in vacuo, and the oily residue was taken up in dichloromethane. The solution was washed with an aqueous 5% HCl solution (2×200 ml), water (2×200 ml) and brine (1×200 ml). The combined organic layers were dried (MgSO4) and the solvent removed in vacuo yielding the crude product as a yellow oil. The liquid chromatographed from silica gel in pentane. Elution with pentane gave the product (1b) (20.59 g, 91 %) as a clear liquid: bp 81°-82° C., 1H NMR (200 MHz, CDCl3) c 0.30 (s), 7.23(m).

Workup

  1. additionwas added over a period of 15 min
  2. customthe disappearance of starting material (2 h)
  3. temperatureThe reaction mixture was cooled to room temperature
  4. filtrationfiltered
  5. customto remove salts
  6. concentrationThe filtrate was concentrated in vacuo
  7. washThe solution was washed with an aqueous 5% HCl solution (2×200 ml), water (2×200 ml) and brine (1×200 ml)
  8. dry with materialThe combined organic layers were dried (MgSO4)
  9. customthe solvent removed in vacuo
  10. customyielding the crude product as a yellow oil
  11. customThe liquid chromatographed from silica gel in pentane
  12. washElution with pentane

Sources & evidence

ORD record
ord-1ba586dabf2d4c97a21a0e179ff84ae4
Source dataset
uspto-grants-1995_09
Patent number
US05453169

Reaction notes

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