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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051716Generated: October 26, 2026

2-Methoxyethanol → (2-Methoxyethoxy)acetic acid

https://huagongshe.com/reaction/2051716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantSodiumHCID 5360545—
ReactantPotassium 2-bromoacetateHCID 23681702—
Product(2-Methoxyethoxy)acetic acidHCID 2764270.5%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04182711
Source datasetuspto-grants-1980_01
ORD IDord-92b15df999414c4e9c8214fbd6284eb2
Source noteuspto-grants-1980_01