2-Methoxyethanol → (2-Methoxyethoxy)acetic acid

HRID 2051716Notes

Reaction equation

HRID 2051716 reaction equation
[Na].Br[CH2:3][C:4]([O-:6])=[O:5].[K+].[CH3:8][O:9][CH2:10][CH2:11][OH:12]>>[CH3:8][O:9][CH2:10][CH2:11][O:12][CH2:3][C:4]([OH:6])=[O:5]

Participants

4

Procedure

Sodium (1.15 g.; 50.0 mmoles) was dissolved in 2-methoxyethanol (50 ml.; anhydrous) under N2 at room temperature. The temperature rose to 110° over about a 30 minute period. The pale yellow mixture was cooled to room temperature and to this was added powdered potassium bromoacetate (8.85 g.; 50.0 mmoles) under vigorous stirring. The mixture (suspension) was stirred at room temperature overnight (19 hrs.) under N2. The excess of methoxyethanol was removed in vacuo and the residue diluted with H2O (50 ml.) and neutralized with 1N HCl (50 ml.). After evaporation of water, the residue was extracted with CH2Cl2 (75 ml.×2) and the extracts were evaporated to dryness yielding 5.26 g. of yellowish oil. This oil was distilled under reduced pressure, yielding 2-methoxyethoxyacetic acid (4.72 g.; 35.2 mmoles; yield 70.5%) as a colorless oil: b.p. 98° C./0.3 mm Hg; nmr (CDCl3): δ ppm 3.45 (3H, s, -OCH3), 3.4-3.9 (4H, m, --OCH2CH2O-), 4.22 (2H, s, HO2CCH2O-), 9.74 (1H, br. s., -CO2H); ir (neat) 1750 cm-1 (νc=o --CO2H).

Workup

  1. customrose to 110° over about a 30 minute period
  2. customThe excess of methoxyethanol was removed in vacuo
  3. additionthe residue diluted with H2O (50 ml.)
  4. customAfter evaporation of water
  5. extractionthe residue was extracted with CH2Cl2 (75 ml.×2)
  6. customthe extracts were evaporated to dryness
  7. customyielding 5.26 g
  8. distillationThis oil was distilled under reduced pressure

Sources & evidence

ORD record
ord-92b15df999414c4e9c8214fbd6284eb2
Source dataset
uspto-grants-1980_01
Patent number
US04182711

Reaction notes

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