Iodine → 1-(3-Bromophenyl)octan-1-ol

HRID 1451625Notes

Reaction equation

HRID 1451625 reaction equation
II.[Mg].[CH2:4](Br)[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[Br:12][C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=1)[CH:16]=[O:17].[Cl-].[NH4+]>O1CCCC1>[Br:12][C:13]1[CH:14]=[C:15]([CH:16]([OH:17])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH:18]=[CH:19][CH:20]=1

Participants

7

Conditions

Temperature
65 °C

Procedure

A small amount of iodine was added to a solution (100 ml) of magnesium (9.8 g) in anhydrous tetrahydrofuran and the mixture was stirred at 50° C. until the color of the iodine disappeared. A solution of heptyl bromide in anhydrous tetrahydrofuran (200 ml) was dropwise added thereto over 1 hour. The mixture was stirred at 65° C. for 1 hour and a solution of m-bromobenzaldehyde in anhydrous tetrahydrofuran (200 ml) was dropwise added thereto under ice-cooling. The mixture was stirred at room temperature for 30 minutes. Under ice-cooling, a saturated aqueous ammonium chloride solution (7.3 ml) was added thereto and the mixture was stirred for 1 hour. The insoluble matters were filtered off and the filtrate was concentrated. The concentrate was dissolved in ethyl acetate and the mixture was washed with water. The mixture was dried over magnesium sulfate and the solvent was distilled away. The residue obtained was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=10:1) to give 50.9 g of the subject compound as an oily substance.

Workup

  1. temperatureunder ice-cooling
  2. stirringThe mixture was stirred at room temperature for 30 minutes
  3. temperatureUnder ice-cooling
  4. stirringthe mixture was stirred for 1 hour
  5. filtrationThe insoluble matters were filtered off
  6. concentrationthe filtrate was concentrated
  7. dissolutionThe concentrate was dissolved in ethyl acetate
  8. washthe mixture was washed with water
  9. dry with materialThe mixture was dried over magnesium sulfate
  10. distillationthe solvent was distilled away
  11. customThe residue obtained
  12. customwas purified by silica gel column chromatography (eluent; hexane:ethyl acetate=10:1)

Sources & evidence

ORD record
ord-9cf9b79880bd4f0aa5319c4bc0291750
Source dataset
uspto-grants-1997_02
Patent number
US05604229

Reaction notes

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