Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3,5-Triazine-2,4-diamine, 6-chloro- | HCID 18831 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Cyclohexylmelamine | HCID 134592 | 86% |
Reaction Steps
A mixed solution of 14.5 g (0.1 mol) of 2,4-diamino-6-chloro-1,3,5-triazine which is an intermediate product synthesized in the Reference Example 1, 140 mL of water, and 29.2 g (0.3 mol) of cyclohexylamine was heated while stirring, followed by being reated for 1 hour at reflux temperature. Subsequently, the reaction mixture was added with 40 mL of aqueous solution containing 12 g of sodium hydroxide over 1 hour, followed by aging for 1 hour. Into a reaction mixture obtained, 200 mL of toluene was added, followed by being cooled to room temperature. A crystalline obtained was filtered, followed by washing in order with 100 mL of toluene, and then 100 mL of water, and drying at reduced pressure to obtain 17.9 g (a yield of 86%) of the above-identified compound. Melting point: 151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998573 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-d871804acb604c21a7ba7abe68e09e74 |
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| Source note | uspto-grants-1999_12 |
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