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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771278Generated: November 3, 2026

Toluene → 2-(3,5-ditert-butyl-4-hydroxy-benzoyl)-3-dimethylamino-N-methyl-prop-2-enamide

https://huagongshe.com/reaction/1771278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant3-(3,5-DI-Tert-butyl-4-hydroxyphenyl)-N-methyl-3-oxopropanamideHCID 86662706—
SolventMethanolHCID 887—
Product2-(3,5-ditert-butyl-4-hydroxy-benzoyl)-3-dimethylamino-N-methyl-prop-2-enamideHCID 8666270898.5%

Reaction Steps

A 100-mL round bottom flask was charged with 3-(3,5-ditert-butyl-4-hydroxy-phenyl)-N-methyl-3-oxo-propanamide (3.05 mg, 10 mmol) and toluene (20 mL). The mixture was heated and to the resulting hot solution was added N,N-dimethylformamide dimethyl acetal (1.50 mL, 11.3 mmol) with evolution of methanol. The mixture was stirred for 5 h without further heating then evaporated to an oil that was taken up in ethyl acetate (50 mL). The resulting solution was washed with water (4×50 mL) then with brine (20 mL), dried with sodium sulfate and evaporated to an oil and then further dried to a solid foam that was kept under high vacuum to reach a constant weight, then ground to a fine powder to afford 3.55 g of the title compound (98%). TLC (ethyl acetate) Rf 0.09. This material, and especially the equivalent material derived from N,N-dimethylacetamidine dimethyl acetal, is readily hydrolyzed to the starting material. It is therefore advisable to use the condensation product directly and immediately after solvent removal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249107B2
Source datasetuspto-grants-2016_02
ORD IDord-754850e2be1d4b1faad3e1b172125155
Source noteuspto-grants-2016_02