Lithium hydroxide, monohydrate → 4-(2,4-Dichlorophenoxy)butyric acid

HRID 1434648Notes

Reaction equation

HRID 1434648 reaction equation
[Cl:1][C:2]1[CH:16]=[C:15]([Cl:17])[CH:14]=[CH:13][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][C:8]([O:10]CC)=[O:9].O[Li].O>C1COCC1.O>[Cl:1][C:2]1[CH:16]=[C:15]([Cl:17])[CH:14]=[CH:13][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9]

Participants

5

Reactant 2

HCID 168937Lithium hydroxide, monohydrateHCID 12375252Ethyl 4-(2,4-dichloro-phenoxy)butanoate

Product 1

HCID 14894-(2,4-Dichlorophenoxy)butyric acidYield 74.3%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

To a solution of ethyl 4-(2,4-dichlorophenoxy)-butyrate (57 g, crude from last step, about 0.2 mol) in THF (500 mL) and water (500 mL) was added LiOH.H2O (12.6 g, 0.3 mol), and the reaction mixture was stirred for 5 h at RT. The mixture was washed with Et2O (3×200 mL), and the aqueous layer was acidified by addition of HCl (20%) to pH ˜2. The mixture was extracted with EtOAc (3×400 mL), the combined organic extracts were washed with water and brine, dried over Na2SO4 and concentrated in vacuo to give the butyric acid (37 g, 74.3% from 2,4-dichlorophenol) as a white solid. 1H-NMR (CDCl3): δ 7.36 (d, 1H, J=8.8 Hz), 7.18 (dd, 1H, J1=8.8 Hz, J2=2.4 Hz), 6.84 (d, 1H, J=8.8 Hz), 4.07 t, 2H, J=7.2 Hz), 2.64 (t, 2H, J=7.2 Hz), 2.17 (p, 2H, J=6.4 Hz).

Workup

  1. washThe mixture was washed with Et2O (3×200 mL)
  2. additionthe aqueous layer was acidified by addition of HCl (20%) to pH ˜2
  3. extractionThe mixture was extracted with EtOAc (3×400 mL)
  4. washthe combined organic extracts were washed with water and brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-a10f212824454fd0991fb8e89a7d5ed6
Source dataset
uspto-grants-2009_11
Patent number
US07615563B2

Reaction notes

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