Hydrochloric Acid → Ethyl 2-(4-hydroxyphenoxy)acetate

HRID 1602544Notes

Reaction equation

HRID 1602544 reaction equation
[C:1]1([CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1)[OH:2].Br[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12].[OH-].[Na+].Cl>CN(C=O)C.O>[OH:2][C:1]1[CH:8]=[CH:7][C:5]([O:6][CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:4][CH:3]=1

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 785HydroquinoneHCID 7748Ethyl bromoacetateHCID 14798Sodium Hydroxide

Product 1

HCID 13187337Ethyl 2-(4-hydroxyphenoxy)acetateYield 13.4%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Conditions

Temperature
0 °C

Procedure

To a mixture of hydroquinone(24 g, 0.22 mol) and ethyl bromoacetate(24 mL, 0.22 mol) in DMF(300 mL) was added 10M aq. NaOH(22 mL, 0.22 mol). The mixture was stirred at 0° C. for 1 h, diluted with H2O, acidified with 6M aq. HCl and extracted with EtOAc. The EtOAc extract was dried(anhydrous MgSO4) and concentrated in vacuo. The residue was swished with Et2O to give ethyl 4-hydroxyphenoxyacetate (5.8 g) as a white powder.

Workup

  1. extractionextracted with EtOAc
  2. extractionThe EtOAc extract
  3. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-da404686bf5d4cafb4c9a4a2882a2a38
Source dataset
uspto-grants-1999_11
Patent number
US05981576

Reaction notes

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