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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919808Generated: November 2, 2026

Hydrochloric Acid → HCID 57951114, compound

https://huagongshe.com/reaction/1919808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethoxy)anilineHCID 600848—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-(3-fluorophenyl)-4-oxobutanoic acidHCID 2759124—
SolventDimethylformamideHCID 6228—
ProductHCID 57951114HCID 5795111488.1%

Reaction Steps

Stir 4-(3-fluoro-phenyl)-4-oxo-butyric acid [C.A. 69797-46-2] (J. Med. Chem. (1983) 26 381) (1.96 g, 10 mmol), 4-trifluoromethoxyaniline (1.77 g, 10 mmol) and O-(1H-benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU) (3.5 g, 11 mmol) in dimethylformamide (30 mL). Add triethylamine (2.02 g, 20 mmol). Stir at room temperature for 48 hours. Pour into dilute aqueous HCl (250 mL) and extract into ethyl acetate. Wash the organic phase three times with water, dry over anhydrous magnesium sulfate, evaporate and purify on a silica gel column (dichloromethane-ethyl acetate) to give the titled compound (3.13 g, 88% yield) MS (m/z): 356 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168659B2
Source datasetuspto-grants-2012_05
ORD IDord-5d0a5bf2fbd14c42987d846a48a3f04a
Source noteuspto-grants-2012_05