Trifluoroacetic acid → Ethyl[(4,5-dichloro-2-nitrophenyl)oxy]acetate

HRID 2354316Notes

Reaction equation

HRID 2354316 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[C:5](F)=[CH:4][C:3]=1[Cl:12].[C:13]([O:17][CH2:18][CH3:19])(=[O:16])[CH2:14][OH:15].[F-].[K+].FC(F)(F)C(O)=O>O.CC#N.O.O1CCOCC1>[CH2:18]([O:17][C:13](=[O:16])[CH2:14][O:15][C:5]1[CH:4]=[C:3]([Cl:12])[C:2]([Cl:1])=[CH:7][C:6]=1[N+:8]([O-:10])=[O:9])[CH3:19]

Participants

8

Reactant 4

HCID 6422Trifluoroacetic acidHCID 12184Ethyl GlycolateHCID 522689Potassium FluorideHCID 5339511,2-Dichloro-4-fluoro-5-nitrobenzene

Product 1

HCID 44203104Ethyl[(4,5-dichloro-2-nitrophenyl)oxy]acetateYield 96.2%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 312751,4-DioxaneSolventHCID 18373917Acetonitrile--water (1/1)Solvent

Conditions

Temperature
100 °C

Procedure

1,2-dichloro-4-fluoro-5-nitrobenzene (50 g, 0.238 mol), ethyl glycolate (90.1 mL, 0.952 mol), and potassium fluoride (76.1 g, 1.31 mol) were added to a 1 L round-bottom flask containing 200 mL of anhydrous dioxane. The mixture was magnetically stirred and heated to 100° C. in an oil bath. After two hours, HPLC (Eclipse XDB-C18, 4.6×250 mm, 5 micron, 1-99% CH3CN/H2O with 0.1% trifluoroacetic acid) showed that all of the starting material (Rt=7.5 min) was gone and that one major peak (Rt=7.8 min) had formed. The reaction mixture was poured into 4 L of water, which resulted in precipitation of the product. The solid was filtered off and dried under vacuum to give ethyl[(4,5-dichloro-2-nitrophenyl)oxy]acetate (67.4 g, 0.229 mol, 96%) as a tan solid. MS (ES) m/e 294 [M+H]+.

Workup

  1. customhad formed
  2. customresulted in precipitation of the product
  3. filtrationThe solid was filtered off
  4. customdried under vacuum

Sources & evidence

ORD record
ord-2fa426fcf11247078ba85815428ea13a
Source dataset
uspto-grants-2010_07
Patent number
US07749998B2

Reaction notes

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