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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413050Generated: October 27, 2026

Potassium Carbonate → Methane

https://huagongshe.com/reaction/1413050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1-(2,2-Diethoxyethoxy)-4-methoxybenzeneHCID 251315—
Reactantp-tolylmethyl N-(pyrazine-2-carbonylamino)carbamateHCID 478568—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
ProductMethaneHCID 297—
Product2-(p-Methoxyphenoxy)-3-(dimethylamino)acroleinHCID 54498024—

Reaction Conditions

Temperature0 °C

Reaction Steps

Dry dimethylformamide (20 ml) was added dropwise to a stirred solution of phosphorus oxychloride (18 ml) maintained at a remperature of 0° C. The reaction mixture was allowed to warm to room temperature and p-methoxyphenoxyacetaldehyde diethyl acetal (16 g) was added with stirring. The mixture was cautiously heated with stirring to a temperature of 90° C. and then maintained at that temperature for 6 hr. The mixture was then cooled and poured slowly onto crushed ice (c. 1 kg) and the pH of the solution adjusted to pH10 by the addition, with stirring, of solid potassium carbonate. A benzene (95%)/alcohol (5%) solution (500 ml) was added to the reaction mixture and the total mixture heated just below its boiling point for 2 hr. The mixture was cooled, the organic layer was separated and dried, and the solvent removed by distillation under reduced pressure to give a black oil. The product crystallised from ethanol, after treatment with charcoal, to give 2-(p-methoxyphenoxy)-3-(dimethylamino)-acrolein (6.4 g) which was characterised by p.m.r. spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04248618
Source datasetuspto-grants-1981_02
ORD IDord-23981861004f46439e6b3bde4d86c737
Source noteuspto-grants-1981_02