Acetic Acid → HCID 57424365, compound

HRID 1961349Notes

Reaction equation

HRID 1961349 reaction equation
[OH-].[Na+].[F:3][C:4]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:5]=1[CH:6]=[O:7].[N+:13]([CH3:16])([O-:15])=[O:14].C(O)(=O)C>CO.C(OCC)C>[F:3][C:4]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:5]=1[CH:6]([OH:7])[CH2:16][N+:13]([O-:15])=[O:14]

Participants

7

Reactant 4

HCID 176Acetic AcidHCID 6375NitromethaneHCID 14798Sodium HydroxideHCID 1376632,5-Difluorobenzaldehyde

Product 1

HCID 57424365HCID 57424365, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolvent2×HCID 3283Diethyl EtherSolvent

Procedure

To sodium hydroxide (1N, 3 L) and methanol (1500 mL) at 5° C. was added a solution of 2,5-difluorobenzaldehyde (350 g, 2.46 mol) and nitromethane (157 mL, 2.9 mol) in methanol (350 mL) dropwise over a period of 1 h. The reaction mixture was then neutralized with glacial acetic acid (165 mL). Diethyl ether (1500 mL) was added and the layers separated. The organic layer was washed successively with saturated aqueous sodium carbonate solution (1000 mL), and saturated aqueous brine (1000 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated to afford 1-(2,5-difluorophenyl)-2-nitroethanol that was used without further purification in Step B.

Workup

  1. customthe layers separated
  2. washThe organic layer was washed successively with saturated aqueous sodium carbonate solution (1000 mL), and saturated aqueous brine (1000 mL)
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-de012eddd4974d52882fc26e2475db8f
Source dataset
uspto-grants-2013_04
Patent number
US08415297B2

Reaction notes

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