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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056107Generated: November 2, 2026

Triethylamine → HCID 22347316, compound

https://huagongshe.com/reaction/2056107

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 numberUS07332497B2
Source datasetuspto-grants-2008_02
ORD IDord-bf473d6973204c488afb22ba8e9ac45d
Source noteuspto-grants-2008_02