Methanol → 3,3,3-Trifluoro-2-oxopropanoic acid

HRID 1466734Notes

Reaction equation

HRID 1466734 reaction equation
[F:1][C:2]([F:11])([F:10])[C:3](=[O:9])[C:4]([O:6]CC)=[O:5].[OH-].[Na+].CO>C(O)C.O>[F:1][C:2]([F:11])([F:10])[C:3](=[O:9])[C:4]([OH:6])=[O:5]

Participants

6

Procedure

To a solution of ethyl 3,3,3-trifluoro-2-oxopropanoate (5 g, 29.36 mmol) in ethanol (30 ml) was slowly added aqueous sodium hydroxide ((2.35 g, 58.72 mmol, dissolved in water (30 ml)), and stirred for 20 h at room temperature until the starting material was consumed. The reaction mixture was concentrated and the resulting white solid was dissolved in water (100 ml). The aqueous layer was extracted by ethyl acetate (50 ml×2), and then the aqueous layer was adjusted PH to 1˜2 with concentrated HCl, and concentrated to give a white solid. The solid was added to methanol (200 ml) and stirred for overnight, filtered, and the filtrate was concentrated and dried to give the crude product (4.13 g, 99%) as a white solid, used in next step without further purification.

Workup

  1. customwas consumed
  2. concentrationThe reaction mixture was concentrated
  3. dissolutionthe resulting white solid was dissolved in water (100 ml)
  4. extractionThe aqueous layer was extracted by ethyl acetate (50 ml×2)
  5. concentrationconcentrated
  6. customto give a white solid
  7. stirringstirred for overnight
  8. filtrationfiltered
  9. concentrationthe filtrate was concentrated
  10. customdried

Sources & evidence

ORD record
ord-27f5700531104a47b23d5f85784dd2b2
Source dataset
uspto-grants-2015_04
Patent number
US08999985B2

Reaction notes

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