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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897907Generated: October 29, 2026

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

https://huagongshe.com/reaction/897907

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 4° 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, 300 A, 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 numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-181030fa77bd4636bc2196f059564732
Source noteuspto-grants-2005_07