Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897917Generated: October 26, 2026

2-Amino-4-methylphenol → N-(4-Bromophenyl)-5-methyl-1,3-benzoxazol-2-amine

https://huagongshe.com/reaction/897917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylphenolHCID 7264—
ReactantTriethylamineHCID 8471—
Reactant4-Bromophenyl isothiocyanateHCID 16133—
CatalystCopper SulfateHCID 24462—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-Bromophenyl)-5-methyl-1,3-benzoxazol-2-amineHCID 2198582581.2%

Reaction Steps

2-Amino-4-methylphenol (1.15 g, 9.34 mmol) was added to a solution of 4-bromophenyl isothiocyanate (2.00 g, 9.34 mmol) in tetrahydrofuran (35 mL) and the reaction was stirred at room temperature for 16 h. Anhydrous copper (II) sulfate (14.06 g, 88.10 mmol), silica gel (14.06 g), and triethylamine (1.3 mL, 9.34 mmol) were added, and the mixture was stirred at room temperature for 24 h. The reaction was concentrated under reduced pressure and then added to a silica pad and purified using 1:5 ethyl acetate:heptane (2 L) followed by diethyl ether as the eluent to afford N2-(4-bromophenyl)-5-methyl-1,3-benzoxazol-2-amine as a light brown solid (2.30 g, 81%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-01aea736a1b54e418366820b21c6b3aa
Source noteuspto-grants-2005_07