1,6-Dibromohexane → 1-Bromo-7-phenylheptane

HRID 2258272Notes

Reaction equation

HRID 2258272 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][Br:8].[CH2:9]([Mg]Cl)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>O1CCCC1>[Br:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

Participants

4

Conditions

Temperature
0 °C

Procedure

To a stirred solution of 1500 mL (0.15 mol) of 0.1M Li2CuCl4 and 1,6-dibromohexane (456.8 g, 1.87 mol, 1.25 eq) in tetrahydrofuran, at -5 to 0° C., was added a solution of benzyl magnesium chloride (750 mL, 2M in tetrahydrofuran, 1.5 mol) over a 90 min period. The reaction mixture was stirred at 0° C. for 90 min, then quenched carefully with 2.0 L of saturated aqueous ammonium chloride. The internal reaction temperature was kept below 20° C. during the quench. The mixture was stirred for 1 h at room temperature and the layers separated. The organic layer was washed with 20% aqueous sodium chloride (4×500 mL). The organic layer was dried (magnesium sulfate), filtered, and concentrated in vacuo at 45°-50° C. to an amber oil. Purification by fractional vacuum distillation through a 12-inch vacuum-jacketed Vigreux column gave the desired product as a colorless oil (198.2 g, 52%). An analytical sample was prepared by redistillation: bp 123°-124° C. (1.5 mm Hg); FT-IR (neat film) 3100-3000, 3000-2800, 2000-1700, 1604, 1496, 748, 699, 644 cm-1 ; 1H NMR (CDCl3, 400 MHz) δ 7.29-7.16 (m, 5 H), 3.40 (t, 2 H), 2.60 (t, 2 H), 1.88-1.81 (m, 2 H), 1.63-1.60 (m, 2 1.32 (m, 6 H); 13C NMR (CDCl3, 100 MHz) δ 142.7, 128.4, 128.2, 125.6, 35.9, 34.0, 32.8, 31.4, 29.1, 28.6, 28.1. Anal. Calcd for C13H19Br: C, 61.19; H, 7.50; Br, 31.31. Found: C, 61.25; H, 7.59; Br, 31.47.

Workup

  1. customquenched carefully with 2.0 L of saturated aqueous ammonium chloride
  2. customwas kept below 20° C. during the quench
  3. stirringThe mixture was stirred for 1 h at room temperature
  4. customthe layers separated
  5. washThe organic layer was washed with 20% aqueous sodium chloride (4×500 mL)
  6. dry with materialThe organic layer was dried (magnesium sulfate)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo at 45°-50° C. to an amber oil
  9. customPurification
  10. distillationby fractional vacuum distillation through a 12-inch vacuum-jacketed Vigreux column

Sources & evidence

ORD record
ord-e054a23ea51946eb9254c43e05a1feeb
Source dataset
uspto-grants-1997_08
Patent number
US05659084

Reaction notes

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