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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256774Generated: November 1, 2026

Methylparaben → HCID 19027292, compound

https://huagongshe.com/reaction/2256774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylparabenHCID 7456—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloroethoxy)ethanolHCID 12361—
ReactantHCID 19027304HCID 19027304—
SolventAcetonitrileHCID 6342—
ProductHCID 19027292HCID 19027292—

Reaction Steps

These compounds were synthesized by a similar method. The representative synthesis of 4-(2-(2-hydroxyethoxy)ethoxy)benzoate (3) is presented. A solution of 2-(2-chloro ethoxy)ethanol 5.338 grams (0.04 mole) in 50 ml of acetonitrile was added dropwise to a solution of methyl 4-hydroxybenzoate 5.1 grams (0.036 mole) and 23.2 grams (0.168 mole) of powdered anhydrous potassium carbonate in 300 ml of acetonitrile at 80° C. After stirring the reaction mixture under reflux for 12 hours, 250 ml of the acetonitrile was then distilled and 250 ml dichloromethane was added. The reaction mixture was filtered through CELITE® and the solid was washed thoroughly with dichloromethane. Evaporation of the filtrate yielded product in the form of a yellow oil. Purification by flash chromatography on silica gel with 40% diethyl ether in dichloromethane yielded 7.1 g (87%). 1H-NMR (CDCl3, TMS): d=2.62 (s, 1H, --OH), 3.81-4.25 (m, 8H, --(OCH2CH2)2 --), 3.85 (s, 3H, --COOCH3), 6.9 and 7.9 (2d, 4 aromatic protons).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656197
Source datasetuspto-grants-1997_08
ORD IDord-a415f6657ec94900a85e4615e8660e6c
Source noteuspto-grants-1997_08