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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448924Generated: October 31, 2026

Methylamine → N,2,6-trimethylaniline

https://huagongshe.com/reaction/1448924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantAcroleinHCID 7847—
ReactantN-(3-penten-2-yl)-morpholineHCID 3828336—
CatalystPalladiumHCID 23938—
ProductN,2,6-trimethylanilineHCID 136604—

Reaction Conditions

Temperature25 °C

Reaction Steps

14.0 g (0.25 mol) of acrolein is added dropwise at 25° to 30° C. to 23.3 g (0.15 mol) of N-(3-penten-2-yl)-morpholine. The mixture obtained is stirred for 15 hours at 25° C. and subsequently, for further 15 hours at 50° C. Then the mixture is transferred into an autoclave and after addition of 400 ml of a 40% by weight aqueous solution of methylamine and 10.0 g of palladium coal (5%), the whole is heated under a nitrogen pressure of 50 bar for 5 hours at 280° to 290° C. Subsequently the catalyst is separated off by filtration and washed with ether. The filtrate is several times extracted with ether, the combined extracts are dried over magnesium sulphate and the ether is distilled off. Then water is added to the residue and the whole is acidified by addition of hydrochloric acid. The acid solution obtained is extracted with ether and the extract is discarded. Now sodium bicarbonate is added to the acid solution until the mixture shows alkaline reaction and the whole is again extracted with ether. The extract is dried over sodium sulphate and the ether is distilled off. N-methyl-2,6-dimethylaniline is obtained by distillation of the residue at 0.1 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04188341
Source datasetuspto-grants-1980_02
ORD IDord-348401d06bef4724be1c64985eba19a4
Source noteuspto-grants-1980_02