Lithium hydroxide, monohydrate → HCID 67532234, compound

HRID 240350Notes

Reaction equation

HRID 240350 reaction equation
[O:1]=[C:2]1[C:11]([C:12]([O:14]CC)=[O:13])=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]1[CH2:17][O:18][CH2:19][C:20]([F:23])([F:22])[F:21].O.[OH-].[Li+]>C(O)C.O>[O:1]=[C:2]1[C:11]([C:12]([OH:14])=[O:13])=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]1[CH2:17][O:18][CH2:19][C:20]([F:23])([F:21])[F:22]

Participants

5

Procedure

1.5 g (4.54 mmol) of ethyl 2-oxo-1-[(2,2,2-trifluoroethoxy)methyl]-1,2-dihydroquinoxaline-3-carboxylate and 0.28 g (6.81 mmol) of lithium hydroxide monohydrate were dissolved in a solvent mixture of ethanol (30 mL) and water (30 mL), and the solution was stirred for 2 hours at room temperature. The reaction solution was concentrated to a half the original volume, and then water was added to the residue. The mixture was acidified using 10% hydrochloric acid, and then extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated, to obtain 2.4 g (yield: 53%) of 2-oxo-1-[(2,2,2-trifluoroethoxy)methyl]-1,2-dihydroquinoxaline-3-carboxylic acid as a white powder.

Workup

  1. concentrationThe reaction solution was concentrated to a half the original volume
  2. additionwater was added to the residue
  3. extractionextracted with ethyl acetate
  4. washThe organic layer was washed with water
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-1dbf16fd01594fdaa84840b495f8d086
Source dataset
uspto-grants-2014_02
Patent number
US08648075B2

Reaction notes

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