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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | N-(2,2,6,6-tetramethyl-4-piperidylidene)-2-methylallylamine | HCID 20405357 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2,2,6,6-tetramethyl-4-piperidylidene)-2-methyl-1-amino-1-propene | HCID 20405359 | 84.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04506099 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-533194612e1b46cba63b873a91254b78 |
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| Source note | uspto-grants-1985_03 |
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