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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470639Generated: November 3, 2026

3',4'-Dimethoxycinnamic acid → HCID 67395457, compound

https://huagongshe.com/reaction/470639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3',4'-Dimethoxycinnamic acidHCID 16848—
ReactantHCID 178510799HCID 178510799—
SolventTolueneHCID 1140—
ProductHCID 67395457HCID 67395457—

Reaction Steps

To a solution of 0.39 g (1.88 mmol) of 3-(3,4-dimethoxy-phenyl)-acrylic acid (compound of Example 2; Step 1) in 6 mL of toluene, 0.333 g (2.00 mmol) of 1,1-carbonyldiimidazole was added in portions at 25° C. to 30° C. under inert atmosphere. To the thickened mixture, 5 mL of toluene was added and the resulting mixture was stirred at 25° C. to 30° C. for 60 to 90 min. A solution of 2-cyclohexyl-N-hydroxyacetimidamide (compound of Example 44; 0.6 g, 3.8 mmol) in 5 mL of toluene was added to the above reaction mixture at 25° C. to 30° C. The reaction mass was stirred at 25° C. to 30° C. under nitrogen for 12-14 h, followed by stirring at 100° C. to 105° C. for 6-8 h. After completion of the reaction, the reaction mixture was cooled to 25° C. to 30° C. and quenched with 10 mL of chilled water under stirring at 25° C. to 30° C. The organic layer was separated, and the aqueous layer was washed with 5 mL of toluene. The organic layers were combined and washed with 10 mL of 1N HCl solution, 10 mL of 5% sodium bicarbonate solution and 10 mL of 10% sodium chloride solution. The organic layer was distilled completely to obtain a crude residue, which was purified by column chromatography (silica gel, chloroform-methanol) to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629277B2
Source datasetuspto-grants-2014_01
ORD IDord-49388ac227d340048fba09846b77964f
Source noteuspto-grants-2014_01