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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056103Generated: October 30, 2026

Triethylamine → 2-[(4-Bromophenyl)amino]-5-benzoxazolecarbonitrile

https://huagongshe.com/reaction/2056103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Bromophenyl isothiocyanateHCID 16133—
Reactant3-Amino-4-hydroxybenzonitrileHCID 271258—
SolventAcetonitrileHCID 6342—
Product2-[(4-Bromophenyl)amino]-5-benzoxazolecarbonitrileHCID 5903528655.5%

Reaction Steps

To a mixture of 3-amino-4-hydroxybenzonitrile (1.84 g, 0.0137 mol) in acetonitrile (140 mL) was added 4-bromophenyl isothiocyanate (2.93 g, 0.0137 mol) at room temperature. The mixture was stirred for 16 hours at room temperature. Cuprous chloride (1.36 g, 0.0137 mol) and triethylamine (1.9 mL, 0.0137 mol) were added to the reaction mixture. The mixture was stirred for 16 hours at room temperature. The solvent was removed under reduced pressure, and the solid was suspended in methanol. The mixture was filtered through celite pad using methanol. The brownish filtrate was left at 40 for three days. The precipitate was filtered and washed with methanol to yield 2-(4-bromoanilino)-1,3-benzoxazole-5-carbonitrile (2.4 g, 0.0076 mol). RP-HPLC (Delta Pak C18, 5 μm, 300A, 15 cm; 5%-95% acetonitrile—0.1M ammonium acetate over 10 min, 1 mL/min) Rt 11.1 min. MS: MH−: 313

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332497B2
Source datasetuspto-grants-2008_02
ORD IDord-4a6fa57a2f5a4ce29fd7683170b21280
Source noteuspto-grants-2008_02