HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500027Generated: October 28, 2026
HCID 68459425, compound → HCID 68458596, compound
https://huagongshe.com/reaction/500027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68459425 | HCID 68459425 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 68458596 | HCID 68458596 | 95% |
Reaction Steps
Diethyl(methyl)-1,3-cyclohexanediamine, as a mixture of its 2,4-diethyl-6-methyl- and 4,6-diethyl-2-methyl-isomers (3.0 g), Pt(S)/C (0.4 g), Amberlyst-15 (0.4 g), and methyl ethyl ketone (45 g) were charged into a 100 mL metal autoclave at 22° C. The closed autoclave was purged 3 times with 125 psig (9.63×105 Pa) of H2 at 22° C. to remove traces of air. The reaction mixture was then heated at 130° C. under 125 psig (9.63×105 Pa) of H2 for 6 hrs (until no further H2 uptake was observed). The product mixture was cooled to 22° C. and degassed. A diluted product sample was analyzed by GC (100° C. for 5 minutes at 10° C. per minute rate; final temperature, 270° C.). The GC data (normalization method) showed 100% conversion of diethyl(methyl)-1,3-cyclohexanediamine, and a 95-97% yield of N,N′-di-sec-butyl-[diethyl(methyl)-1,3-cyclohexanediamine].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767858B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-5afe1bc2f42b48dbbf4e37249238d098 |
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| Source note | uspto-grants-2010_08 |
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