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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169545Generated: November 2, 2026

Hexylamine → HCID 86053884, compound

https://huagongshe.com/reaction/1169545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexylamineHCID 8102—
ReactantTriethylamineHCID 8471—
Reactant2,4,6-TrichloroborazineHCID 70274—
SolventTolueneHCID 1140—
ProductHCID 86053884HCID 8605388497.3%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07824784B2
Source datasetuspto-grants-2010_11
ORD IDord-7ce447b2f5354f6cadf3fecd2ba93098
Source noteuspto-grants-2010_11