HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277560Generated: October 27, 2026
Ammonia → 2,2,12-Trimethyltridecane-1,11-diamine
https://huagongshe.com/reaction/1277560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | N-(11-Amino-2,2,12-trimethyltrideca-4,8-dien-1-ylidene)hydroxylamine | HCID 71403854 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,2,12-Trimethyltridecane-1,11-diamine | HCID 3018553 | 92.7% |
Reaction Steps
490 g (1.84 moles) of the 2,2-dimethyl-11-isopropyl-11-amino-undeca-4,8-dienal oxime obtained according to Example 5 are dissolved in 2.4 liters of methanol and this solution is filled, together with about 200 g of liquid ammonia, with the addition of 150 g of Raney nickel, into a 6.3 liter steel autoclave. Hydrogen is then injected until the pressure is 100 bars and the mixture is heated to 100° C. with stirring. The mixture is hydrogenated forabout 5 hours under these conditions and cooled and the ammonia and excess hydrogen are then allowed to blow off. Subsequent distillation under a high vacuum yields 436 g (1.705 mols) of 1-isopropyl-10,10-dimethyl-1,11-diaminoundecane in the form of a colourless, water-clear liquid; boiling point 87° C./4 Pa; nD20 =1.46l9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04277621 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-7a07163bef9a4a87a436077c0eb226aa |
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| Source note | uspto-grants-1981_07 |
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