Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Melamine | HCID 7955 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 9795432 | HCID 9795432 | 6.7% |
| Product | HCID 9815571 | HCID 9815571 | 22% |
Reaction Steps
In a stainless steel autoclave of an inner volume of 100 ml, 1.26 g (10 mmol) of melamine, 250 mg of 5% Pd—C catalyst, and 30 ml of 1,4-butanediol were charged. After the inside of the reaction system was sufficiently substituted with nitrogen gas, 10 kg/cm2 of hydrogen gas was introduced under pressure at normal temperature. Then, the temperature was elevated while stirring, and after the temperature reached 260° C., the reaction was carried out at the same temperature for further 2 hours. After cooling, the reaction mixture was taken out and quantitative analysis of the reaction product was performed under the above analytical conditions. As a result, the reaction conversion rate of the starting material melamine was 48.1% and it was confirmed that there were produced only 22.0% of 2,4-diamino-6-(4-hydroxybutylamino)-1,3,5-triazine and 6.7% of 2-amino-4,6-bis (4-hydroxybutylamino)-1,3,5-triazine as the products, and an obvious decrease in activity as compared with the mixed catalyst systems was confirmed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06307046B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-ba1c40ff707b42d09e52a7eea5653870 |
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| Source note | uspto-grants-2001_10 |
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