1-Bromo-4-ethylbenzene → α-(4-Ethylphenyl)-2-(phenylmethoxy)benzenemethanol

HRID 604745Notes

Reaction equation

HRID 604745 reaction equation
[Mg].Br[C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH3:10])=[CH:5][CH:4]=1.[CH2:11]([O:18][C:19]1[CH:26]=[CH:25][CH:24]=[CH:23][C:20]=1[CH:21]=[O:22])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[Cl-].[NH4+]>BrC1C=CC(CC)=CC=1.O1CCCC1>[CH2:11]([O:18][C:19]1[CH:26]=[CH:25][CH:24]=[CH:23][C:20]=1[CH:21]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH3:10])=[CH:5][CH:4]=1)[OH:22])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1

Participants

7

Reactant 4

HCID 153131-Bromo-4-ethylbenzeneHCID 25517Ammonium ChlorideHCID 3447842-(Benzyloxy)benzaldehydeHCID 5462224Magnesium

Product 1

HCID 67069123α-(4-Ethylphenyl)-2-(phenylmethoxy)benzenemethanolYield 101.4%

Reagents, catalysts & solvents 2

HCID 153131-Bromo-4-ethylbenzeneCatalystHCID 8028TetrahydrofuranSolvent3×

Procedure

1-Bromo-4-ethylbenzene (6.69 g, 0.036 mol) was added to a suspension of magnesium (17.2 g) and tetrahydrofuran (50 mL) and heated to reflux. Subsequently, a tetrahydrofuran (300 mL) solution of 1-bromo-4-ethylbenzene (97.9 g, 0.529 mol) was added for two hours at room temperature. After stirred at room temperature for 1.5 hours, the reaction mixture was cooled to 4° C. and a tetrahydrofuran (100 mL) solution of 2-benzyloxybenzaldehyde (100 g, 0.471 mol) was added for one hour. After stirred for two hours, the reaction mixture was poured into a saturated ammonium chloride aqueous solution. After the mixture was extracted with ethyl acetate, the organic phase was washed with brine and then dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=95:5) to obtain (2-benzyloxyphenyl)(4-ethylphenyl)methanol (152 g) as a colorless solid.

Workup

  1. temperatureheated to reflux
  2. temperaturethe reaction mixture was cooled to 4° C.
  3. stirringAfter stirred for two hours
  4. extractionAfter the mixture was extracted with ethyl acetate
  5. washthe organic phase was washed with brine
  6. dry with materialdried with anhydrous magnesium sulfate
  7. filtrationAfter the desiccant was filtered off
  8. customthe residue obtained
  9. customby evaporating the solvent under reduced pressure
  10. customwas purified by silica gel column chromatography (hexane:ethyl acetate=95:5)

Sources & evidence

ORD record
ord-504a6e10b67a44f99bff5e160191ec8b
Source dataset
uspto-grants-2011_03
Patent number
US07910619B2

Reaction notes

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