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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247965Generated: November 1, 2026

Iodoethane → N-(3-acetylphenyl)-N-ethyl-4-methylbenzenesulfonamide

https://huagongshe.com/reaction/1247965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantN-(3-Acetylphenyl)-4-methylbenzenesulfonamideHCID 220585—
ReactantSodium MethoxideHCID 10942334—
SolventDimethylformamideHCID 6228—
ProductN-(3-acetylphenyl)-N-ethyl-4-methylbenzenesulfonamideHCID 20280466—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 29 g portion of N-(3-acetylphenyl)-4-methylbenzenesulfonamide was dissolved in 250 ml of dimethylformamide with stirring. This mixture was treated with 6.5 g of sodium methoxide and stirred for 30 minutes, then 20 g of ethyl iodide was added. This mixture was stirred at room temperature for one hour, then at reflux for 5 hours. The dimethylformamide was removed in vacuo, the residue shaken with 150 ml of water, the mixture adjusted to pH 4 with 10N sodium hydroxide and then cooled to 0° C. The precipitate was collected, washed twice with water and then air dried, giving 31.5 g of N-(3-acetylphenyl)-N-ethyl-4-methylbenzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04521422
Source datasetuspto-grants-1985_06
ORD IDord-79a78215d79d4734b818b9fb08dcdda8
Source noteuspto-grants-1985_06