HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955965Generated: November 1, 2026
Carbon Dioxide → Methyl-bis(2,2,6,6-tetramethylpiperidin-4-yl)amine
https://huagongshe.com/reaction/1955965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | N-(9H-Fluoren-9-ylacetyl)-S-methylcysteine | HCID 128652 | — |
| Reactant | 2,2,6,6-Tetramethyl-N-(2,2,6,6-tetramethyl-4-piperidinyl)-4-piperidinamine | HCID 566708 | — |
| Product | Methyl-bis(2,2,6,6-tetramethylpiperidin-4-yl)amine | HCID 19073312 | 49% |
Reaction Steps
1. A 200 ml sulfonation flask is charged with 40.48 g (0.14 mol) of bis(2,2,6,6-tetramethyl-piperidin-4-yl)amine [EP-A-336 895, Ciba-Geigy] and 11.4 g (0.14 mol) of a 36% aqueous solution of formaldehyde. 25.8 g (0.56 mol) of formic acid are added dropwise at room temperature. The temperature in the flask rises to 70° C. with evolution of CO2. The reaction mixture is stirred until it has cooled to room temperature. The aqueous phase is then saturated with potassium carbonate and the reaction mixture is extracted three times with chloroform. The organic phases are combined, dried over potassium carbonate and concentrated on a vacuum rotary evaporator. Chromatography of the residue over silica gel using the solvent system hexane/dichloromethane 9:1+5% triethylamine gives 21 g (49%) of the methyl-bis(2,2,6,6-tetramethyl-piperidin-4-yl)amine, m.p. 51°-53° C., in the form of a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05777113 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-38705344413e4fcea67ac93f5bfdb14a |
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| Source note | uspto-grants-1998_07 |
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