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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427682Generated: October 30, 2026

Ethyl Acetate → 5-Fluoro-2-(4-trifluoromethyl-benzyl)-7-trifluoromethyl-2,3-dihydro-isoindol-1-one

https://huagongshe.com/reaction/2427682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Trifluoromethyl)benzylamineHCID 76804—
Reactant4-Fluoro-2-bromomethyl-6-trifluoromethyl-benzoic acid methyl esterHCID 67251868—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product5-Fluoro-2-(4-trifluoromethyl-benzyl)-7-trifluoromethyl-2,3-dihydro-isoindol-1-oneHCID 57949479323.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-fluoro-2-bromomethyl-6-trifluoromethyl-benzoic acid methyl ester (0.100 g, 0.32 mmol), 4-trifluoromethyl-benzylamine (0.06 mL, 0.42 mmol), and K2CO3 (0.088 g, 0.64 mmol) in toluene (4 mL) was heated with stirring at 100° C. for 2 h. Workup and silica gel column chromatography using 30% ethyl acetate in hexane afforded 5-fluoro-2-(4-trifluoromethyl-benzyl)-7-trifluoromethyl-2,3-dihydro-isoindol-1-one (0.39 g, 33%). 1H NMR (300 MHz, CDCl3): δ (ppm) 4.34 (s, 2H), 4.84 (s, 2H) 7.20-7.50 (m, 6H). GC-MS: m/z 377 (M)+, 356 (M−21)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968570B2
Source datasetuspto-grants-2011_06
ORD IDord-b0a023b2eeae4bf180d348956841dab8
Source noteuspto-grants-2011_06