Sodium Hydroxide → 5-Chloro-2-fluoro-4-methylbenzoic acid

HRID 508422Notes

Reaction equation

HRID 508422 reaction equation
[Cl:1][C:2]1[C:3]([CH3:13])=[CH:4][C:5]([F:12])=[C:6]([CH:11]=1)[C:7]([O:9]C)=[O:8].[OH-].[Na+]>O1CCOCC1.O>[Cl:1][C:2]1[C:3]([CH3:13])=[CH:4][C:5]([F:12])=[C:6]([CH:11]=1)[C:7]([OH:9])=[O:8]

Participants

4

Procedure

To a stirred solution of methyl 5-chloro-2-fluoro-4-methylbenzoate (Preparation 12, 340 mg, 1.68 mmol) in dioxane/water (5:1, 12 mL) was added a sodium hydroxide solution (5 M, 1.63 mL, 8.39 mmol). The reaction mixture was stirred at room temperature for 18 hours and then evaporated in vacuo. The resulting residue was suspended in water and extracted with diethyl ether (3×20 mL). The aqueous layer was separated, cooled in an ice bath, acidified with aqueous hydrochloric acid (6 M) and then extracted with EtOAc (30 mL). The combined organics were washed with brine (2×20 mL), dried over sodium sulphate, filtered and evaporated in vacuo to yield the title compound as a white solid (266 mg, 84%).

Workup

  1. customevaporated in vacuo
  2. extractionextracted with diethyl ether (3×20 mL)
  3. customThe aqueous layer was separated
  4. temperaturecooled in an ice bath
  5. extractionextracted with EtOAc (30 mL)
  6. washThe combined organics were washed with brine (2×20 mL)
  7. dry with materialdried over sodium sulphate
  8. filtrationfiltered
  9. customevaporated in vacuo

Sources & evidence

ORD record
ord-f7de0fe7e88e43f68f8805cfe77bd172
Source dataset
uspto-grants-2015_08
Patent number
US09096500B2

Reaction notes

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