Methylparaben → Methyl 4-(4-phenylbutoxy)benzoate

HRID 52607

Reaction equation

HRID 52607 reaction equation
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.C[O-].[Na+].[C:15]1([CH2:21][CH2:22][CH2:23][CH2:24]Br)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[OH-].[Na+]>CN(C=O)C>[C:15]1([CH2:21][CH2:22][CH2:23][CH2:24][O:1][C:2]2[CH:3]=[CH:4][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:10][CH:11]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

6

Procedure

A solution of methyl 4-hydroxybenzoate (13.4 kg, 88 mol) in DMF (52 L) was added dropwise to a mixture of NaOMe (4.8 kg, 89 mol) and DMF (50 L) at room temperature under a gentle stream of nitrogen. The reaction mixture was heated at 60°-70° for 1 hr with stirring and then cooled to room temperature. To this mixture was added dropwise a solution of 4-phenylbutyl bromide (16.92 kg, 79.4 mol) in DMF (5 L). The resulting mixture was heated at 60°-70° for 1 hr with constant stirring and cooled to room temperature. After an addition of 1N-NaOH (110 L) was added, and the product was extracted twice with ethyl acetate (50 L and 80 L). The extracts were washed with 1N-NaOH (110 L) and saturated brine (20 L) successively, and then concentrated to dryness in vacuo to give the title compound in quantitative yield.

Workup

  1. temperatureThe reaction mixture was heated at 60°-70° for 1 hr
  2. temperatureThe resulting mixture was heated at 60°-70° for 1 hr
  3. stirringwith constant stirring
  4. temperaturecooled to room temperature
  5. additionwas added
  6. extractionthe product was extracted twice with ethyl acetate (50 L and 80 L)
  7. washThe extracts were washed with 1N-NaOH (110 L) and saturated brine (20 L) successively
  8. concentrationconcentrated to dryness in vacuo

Sources & evidence

ORD record
ord-1459c7ee68434c8ab950324f3d1949b0
Source dataset
uspto-grants-1997_04
Patent number
US05616721

Linked notes

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