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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358842Generated: October 31, 2026

Dimethylformamide → HCID 54500603, compound

https://huagongshe.com/reaction/358842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAcrylic AcidHCID 6581—
ReactantSodium AcetateHCID 517045—
ReactantN-(4-chloro-2-iodophenyl)acetamideHCID 15113903—
CatalystTriphenylphosphineHCID 11776—
CatalystPalladium ChlorideHCID 24290—
SolventWaterHCID 962—
ProductHCID 54500603HCID 5450060385.7%

Reaction Conditions

Temperature115 °C

Reaction Steps

To a 200-ml flask were added 40 ml of DMF, 20 g (0.0677 mole) of 2-acetylamino-5-chloroiodobenzene, 5.85 g (0.0812 mole) of acrylic acid, 7.77 g (0.0947 mole) of anhydrous sodium acetate, 10 mg of palladium chloride and 30 mg of triphenylphosphine. This mixture was stirred at 115° C. for 5 hours and poured into 200 ml of water, and then a large amount of crystal precipitated. Sodium hydroxide was added to this aqueous solution containing the crystal while stirring the solution as it was, until the pH of the solution became 9.0. Then, the crystal dissolved in the solution to obtain a uniform solution. Thereafter, 2 g of activated carbon was added to the solution, and after stirring at room temperature for 15 minutes, the insoluble matter was filtered off. The filtrate was acidified to a pH of 1.5 with conc. hydrochloric acid, and then white crystal precipitated. This crystal was filtered off and vacuum-dried to obtain 13.9 g of 2-acetylamino-5-chlorocinnamic acid. The yield was 85.2% of the theoretical value, and the melting point was 243° to 245° C. The 1H-NMR and IR of this compound were as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997972
Source datasetuspto-grants-1991_03
ORD IDord-dbac2e19be34477a961b82b2cff056d1
Source noteuspto-grants-1991_03