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Hydrochloric Acid → 2-(4-(2,2-Difluoroethoxy)phenyl)acetic acid

HRID 1803204
Notes
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Reaction equation

HRID 1803204 reaction equation
[H-].[Na+].[OH:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([O:13]C)=[O:12])=[CH:6][CH:5]=1.FC(F)(F)S(O[CH2:21][CH:22]([F:24])[F:23])(=O)=O.[Li+].[OH-].O.Cl>C1COCC1>[F:23][CH:22]([F:24])[CH2:21][O:3][C:4]1[CH:5]=[CH:6][C:7]([CH2:10][C:11]([OH:13])=[O:12])=[CH:8][CH:9]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 168937Lithium hydroxide, monohydrateHCID 518900Benzeneacetic acid, 4-hydroxy-, methyl esterHCID 27740892,2-Difluoroethyl trifluoromethanesulfonate

Product 1

HCID 196227772-(4-(2,2-Difluoroethoxy)phenyl)acetic acid
Yield 108%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
0 °C

Procedure

Step AX (1): Sodium hydride (60% in mineral oil, 1.70 g, 42.5 mmol) was carefully added portionwise to a solution of methyl 2-(4-hydroxyphenyl)acetate (7.06 g, 42.5 mmol) in THF (200 mL) maintained at 0° C. The cold bath was removed and the mixture was allowed to warm to rt and stir for 30 min. A solution of 2,2-difluoroethyl trifluoromethanesulfonate (10.0 g, 46.7 mmol) in THF (20 mL) was added and the resulting mixture was left to stir for 18 h. A solution of 2 N LiOH/water (40 mL, 80 mmol) was added to the crude reaction mixture and the resulting solution stirred at rt for 3 h. The reaction mixture was poured into 1 N HCl (250 mL) and extracted with Et2O. The combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated. The residue was triturated with hexane. The crystalline solid was collected by vacuum filtration to afford 2-(4-(2,2-difluoroethoxy)phenyl)acetic acid (9.90 g, 45.8 mmol, 108% yield) as an off-white solid. LC-MS (M−H)− 215.1. 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 7.23 (d, J=8.5 Hz, 2 H), 6.89 (d, J=8.5 Hz, 2 H), 6.03-6.14 (m, 1 H), 4.18 (td, J=13.0, 4.1 Hz, 2 H), 3.61 (s, 2 H).

Workup

  1. customThe cold bath was removed
  2. temperatureto warm to rt
  3. waitthe resulting mixture was left
  4. stirringto stir for 18 h
  5. customreaction mixture
  6. stirringthe resulting solution stirred at rt for 3 h
  7. extractionextracted with Et2O
  8. washThe combined organic layers were washed with brine
  9. dry with materialdried (MgSO4)
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customThe residue was triturated with hexane
  13. filtrationThe crystalline solid was collected by vacuum filtration

Sources & evidence

ORD record
ord-441b15bc2fe34a8d97dac787ec477e02
Source dataset
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08349880B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes