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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306136Generated: October 27, 2026

Formamide → 4-Acetylbenzamide

https://huagongshe.com/reaction/2306136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
Reactantp-BromoacetophenoneHCID 7466—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
CatalystHCID 178418476HCID 178418476—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-AcetylbenzamideHCID 11159497—

Reaction Conditions

Temperature120 °C

Reaction Steps

0.122 g of bis(triphenylphosphine)-palladium(II) chloride, 3.439 g of 4-bromoacetophenone, 3.12 g of formamide, 2.37 g of 4-dimethylamino-pyridine and 20 ml of 1-methyl-2-pyrrolidinone are placed in a 200 ml glass autoclave. The autoclave is closed, flushed with nitrogen three times and then 5 bars carbon monoxide are applied. The reaction mixture is heated to 120° C. and stirred for 18 hours. It is then cooled, and the solution is diluted with ethyl acetate and water, and extracted. The aqueous phase is extracted by shaking 3 times with ethyl acetate, and afterwards the organic phases are collected, dried over magnesium sulphate and concentrated. The oil obtained is chromatographed over silica gel. The yield of title compound is 35% (part of the product remains in the water phase).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441233B1
Source datasetuspto-grants-2002_08
ORD IDord-7ec90f09f80f4d00b4a81c88f16b120d
Source noteuspto-grants-2002_08