Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexylamine | HCID 8102 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4,6-Trichloroborazine | HCID 70274 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86053884 | HCID 86053884 | 97.3% |
Reaction Steps
B,B′,B″-trichloroborazine (15 g) was dissolved into sufficiently dewatered toluene (100 mL) and a mixture solution of n-hexyl amine (37 g), triethyl amine (25 g) and toluene (100 mL) was dropped over 1 hour at room temperature. After completion of the drop-wise addition, the solution was stirred at 25° C. for 3 hours and further at 60° C. for 3 hours. An amine-HCl salt generated was removed by filtration, followed by removal of the solvent and unreacting amine under reduced pressure to obtain B,B′,B″-tris(hexylamino)borazine as yellow viscous liquid (30 g). Thus obtained compound was further stirred in xylene at 130° C. for 3 hours to proceed polycondensation reaction. After the reaction, the solvent is removed under reduced pressure to obtain a borazine ring-containing compound 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07824784B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-7ce447b2f5354f6cadf3fecd2ba93098 |
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| Source note | uspto-grants-2010_11 |
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