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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897911Generated: October 31, 2026

Triethylamine → HCID 22347316, compound

https://huagongshe.com/reaction/897911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Bromophenyl isothiocyanateHCID 16133—
Reactant2-Amino-4-(trifluoromethoxy)phenolHCID 2737729—
CatalystCopper SulfateHCID 24462—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22347316HCID 2234731651.1%

Reaction Steps

To a mixture of 2-amino-4-(trifluoromethoxy)phenol (0.9 g, 0.0047 mol) in tetrahydrofuran (60 mL) was added 4-bromophenyl isothiocyanate (1 g, 0.0047 mol) at room temperature. The mixture was stirred for 16 hours at room temperature. Anhydrous copper sulfate (7.1 g, 0.0443 mol, 9.43 eq.), triethylamine (0.67 mL, 0.0047 mol, 1 eq.), and silica gel (8.5 g) were added to the reaction mixture. The mixture was stirred for 4 hours at room temperature. The solvent was removed under reduced pressure. The mixture was filtered through silica gel pad using 25% ethyl acetate/n-heptane as a mobile phase to give orange colored solid. The solid was purified by flash column chromatography on silica using 0%-25% ethyl acetate/n-heptane as a mobile phase. The solvent was removed, and the residue was triturated with n-heptane to give N2-(4-bromophenyl)-5-(trifluoromethoxy)-1,3-benzoxazol-2-amine (0.9 g, 0.0024 mol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-b2432c1308364790999af9f0f9b7243c
Source noteuspto-grants-2005_07