Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599108Generated: November 4, 2026

Hydrochloric Acid → (2-(2-Methoxyethoxy)ethoxy)acetic acid

https://huagongshe.com/reaction/1599108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylene glycol monomethyl etherHCID 8178—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventWaterHCID 962—
Product(2-(2-Methoxyethoxy)ethoxy)acetic acidHCID 8524184.6%

Reaction Steps

A 0.5 g quantity of platinum oxide is hydrogenated in 60 ml of water at 25° C. and atmospheric pressure until the uptake of hydrogen ceases. To the resultant mixture is added a mixture of 0.6 g (7.14 mmoles) of sodium bicarbonate and 1.0 g (6.1 mmoles) of triethylene glycol monomethyl ether dissolved in 20 mL of water. Air is bubbled through the above mixture for 4 hr following the consumption of staging material by TLC. The reaction is then filtered though Celite and the Celite washed with water. The combined washes are treated with 7.2 mL (7.2 mmoles) of 1N hydrochloric acid and the resultant solution freeze-dried. The residue is washed with acetone and filtered. The filtrate is evaporated to dryness under vacuum. The residual oil is chromatographed over 100 g of CC-4 silica gel eluted with (50-50)acetone-methylene chloride, collecting 20 mL fractions. Concentration of fractions 11-16 gives 0.92 g of the desired 3,6,9-trioxadecanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739350
Source datasetuspto-grants-1998_04
ORD IDord-14f7b9a478c54cdda34d28627377fd52
Source noteuspto-grants-1998_04