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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897947Generated: October 29, 2026

Triethylamine → N2-(4-bromophenyl)-7-isopropyl-1,3-benzoxazol-2-amine

https://huagongshe.com/reaction/897947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-Bromophenyl isothiocyanateHCID 16133—
Reactant2-Amino-6-isopropylphenolHCID 14684982—
CatalystCopper SulfateHCID 24462—
SolventTetrahydrofuranHCID 8028—
ProductN2-(4-bromophenyl)-7-isopropyl-1,3-benzoxazol-2-amineHCID 2234713591%

Reaction Steps

A solution of 2-amino-6-isopropylphenol (0.354 g, 2.34 mmol) and 4-bromophenylisothiocyanate (0.500 g, 2.34 mmol) in tetrahydrofuran (35 mL) was stirred at room temperature for 3 h. Anhydrous copper (II) sulfate (3.361 g, 21.06 mmol), silica gel (3.361 g), and triethylamine (0.236 g, 0.33 mL, 2.34 mmol) were added, and the mixture stirred at room temperature for 18 h. The reaction mixture was filtered through a pad of Celite and the washed with diethyl ether (3×50 mL). The filtrate was concentrated to afford a brown solid. The solid material was applied to silica gel and passed through a pad a silica gel along with ethyl acetate (3×50 mL). The filtrate was concentrated to afford N2-(4-bromophenyl)-7-isopropyl-1,3-benzoxazol-2-amine (0.702 g, 91%). RP-HPLC Rt 18.066 min, 86% purity (5% to 85% acetonitrile/0.1M aqueous ammonium acetate, buffered to pH 4.5, over 20 min at 1 mL/min; λ=254 nm; Deltapak C18, 300 Å, 5 μm, 150×3.9 mm column); m/z 333 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-31a65eb9c2184af09e1d502cb1c8c288
Source noteuspto-grants-2005_07