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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463388Generated: October 27, 2026

Methyl iodide → N-methyl-N-(3-bromophenyl)-3,3-dimethyl-acrylamide

https://huagongshe.com/reaction/1463388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantN-3,3-Dimethylacryloyl-3-bromoanilineHCID 19177475—
SolventDimethyl SulfoxideHCID 679—
ProductN-methyl-N-(3-bromophenyl)-3,3-dimethyl-acrylamideHCID 1993549185.2%

Reaction Steps

28.7 g of powdered potassium hydroxide were suspended in 300 ml of dimethyl sulfoxide and a solution of 32.6 g of N-(3-bromophenyl)-3,3-dimethyl-acrylamide in 200 ml of dimethylsulfoxide (DMSO) was added dropwise thereto. The mixture was stirred at room temperature for 30 minutes and subsequently a solution of 27.5 g of methyl iodide in 150 ml of DMSO was added dropwise thereto. After 2.5 hours the mixture was poured on to 1 l of ice/water and extracted with ethyl acetate. The organic phase was washed repeatedly with water, dried and evaporated. The oily residue was distilled in a high vacuum. There were obtained 29.3 g of N-methyl-N-(3-bromophenyl)-3,3-dimethyl-acrylamide as a slightly yellow oil, boiling point 112°-114° C./67 Pa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300522
Source datasetuspto-grants-1994_04
ORD IDord-a1effbf4a9c9434390d42734cd96a8f5
Source noteuspto-grants-1994_04