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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427569Generated: October 26, 2026

Phthalimidine → 2-(4-Trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one

https://huagongshe.com/reaction/2427569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimidineHCID 10199—
ReactantCesium carbonateHCID 10796—
Reactant18-Crown-6HCID 28557—
Reactant1-(Bromomethyl)-4-(trifluoromethoxy)benzeneHCID 142785—
SolventAcetoneHCID 180—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product2-(4-Trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-oneHCID 5794968981%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2,3-dihydro-isoindol-1-one (0.133 g, 1 mmol), 1-bromomethyl-4-trifluoromethoxy-benzene (0.306 g, 1.2 mmol), Cs2CO3 (0.816 g, 2.5 mmol), and 18-crown-6 (0.026 g, 0.1 mmol) in acetone (5 mL) was stirred at 70° C. for 16 h. Workup and silica gel column chromatography using 30% ethyl acetate in hexane afforded 2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.125 g, 81%). 1H NMR (300 MHz, CDCl3): δ (ppm) 4.28 (s, 2H), 4.82 (s, 2H), 7.16 (d, 2H), 7.32-7.52 (m, 5H), 7.90 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968570B2
Source datasetuspto-grants-2011_06
ORD IDord-c1097711188b469c949d21e765748648
Source noteuspto-grants-2011_06