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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415643Generated: October 27, 2026

Dimethylamine → N-(4-butyl-2-nitrophenyl)-2-(dimethylamino)acetamide

https://huagongshe.com/reaction/1415643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantN-(4-n-butyl-2-nitrophenyl)-2-bromoacetamideHCID 21482995—
SolventEthanolHCID 702—
ProductN-(4-butyl-2-nitrophenyl)-2-(dimethylamino)acetamideHCID 21482988—

Reaction Steps

A suspension of N-(4-n-butyl-2-nitrophenyl)-2-bromoacetamide (41 g) in ethanol (200 ml) was treated with a solution of dimethylamine in ethanol (90 ml of 20% w/w). The mixture was refluxed for one hour and the ethanol was evaporated off. Water (100 ml) was added and the mixture extracted with diethyl ether (3 × 200 ml). The extract was dried over magnesium sulphate, filtered and evaporated to give N-(4-n-butyl-2-nitrophenyl)-2-dimethylaminoacetamide as a yellow oil which was used without further purification in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005217
Source datasetuspto-grants-1977_01
ORD IDord-a8c4d1c2cf4b458dbbf5cebc50591543
Source noteuspto-grants-1977_01