Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387360Generated: October 31, 2026

Ethylene Glycol → 2-(2,5-dimethylphenoxymethyl)phenyl 1,3-dioxolan-2-yl ketone O-methyloxime

https://huagongshe.com/reaction/1387360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantBenzeneHCID 241—
Reactant2-(2,5-Dimethylphenoxymethyl)-alpha-methoxyiminophenylacetaldehydeHCID 53861051—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventSodium chloride; waterHCID 57417360—
Product2-(2,5-dimethylphenoxymethyl)phenyl 1,3-dioxolan-2-yl ketone O-methyloximeHCID 5407223187.9%

Reaction Steps

Benzene (4 ml), ethylene glycol (0.12 g, 2.0 mmol) and p-toluenesulfonic acid monohydrate (0.01 g, 0.05 mmol) were added to 2-(2,5-dimethylphenoxymethyl)-α-methoxyiminophenylacetaldehyde (0.3 g, 1.0 mmol), and the mixture was subjected to azeotropic dehydration for 2 hours. After completion of the reaction, half-saturated brine (100 ml) was added, and the mixture was extracted with dichloromethane (50 ml) twice. The extracts were dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetatein-hexane) to give 2-(2,5-dimethylphenoxymethyl)phenyl 1,3-dioxolan-2-yl ketone O-methyloxime (0.30 g, yield 87.9%) as colorless crystals. mp 136-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268312B1
Source datasetuspto-grants-2001_07
ORD IDord-de053d817d9e4b46b72cf4e8af737a6a
Source noteuspto-grants-2001_07