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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164690Generated: October 26, 2026

Dimethyl Sulfoxide → N-(2,2,6,6-tetramethyl-4-piperidylidene)-2-methyl-1-amino-1-propene

https://huagongshe.com/reaction/2164690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantN-(2,2,6,6-tetramethyl-4-piperidylidene)-2-methylallylamineHCID 20405357—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTolueneHCID 1140—
ProductN-(2,2,6,6-tetramethyl-4-piperidylidene)-2-methyl-1-amino-1-propeneHCID 2040535984.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

162.5 g of the N-(2,2,6,6-tetramethyl-4-piperidylidene)-2-methylallylamine are dissolved in 162 ml of toluene in a 500 ml three-necked flask with reflux condenser, and 4.86 g of potassium tert-butylate are added. To the reaction mixture are then added, with stirring, 50 ml of dimethyl sulfoxide, and stirring is maintained at 50° C. for 8 hours. The organic phase is afterwards extracted with 100 ml of distilled water, and the organic part, after separation of the solvent, is distilled to yield 136.9 g of N-(2,2,6,6-tetramethyl-4-piperidylidene)-2-methyl-1-amino-1-propene as a colourless liquid, b.p. 56° C. at 40 Pa (82% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04506099
Source datasetuspto-grants-1985_03
ORD IDord-533194612e1b46cba63b873a91254b78
Source noteuspto-grants-1985_03