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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427743Generated: November 2, 2026

2,2,2-Trifluoroethanol → HCID 67251522, compound

https://huagongshe.com/reaction/2427743

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantCesium carbonateHCID 10796—
ReactantHCID 67251198HCID 67251198—
Catalystpalladium(II) acetateHCID 167845—
Catalyst(1,1'-Binaphthalen)-2-yldi-tert-butylphosphineHCID 2734941—
SolventTolueneHCID 1140—
ProductHCID 67251522HCID 6725152264%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 5,7-dichloro-2-(4-bromo-benzyl)-2,3-dihydro-isoindol-1-one (0.148 g, 0.4 mmol), palladium(II) acetate (0.004 g, 0.02 mmol), rac-2-(di-t-butylphosphino)-1,1′-binaphthyl (0.009 g, 0.025 mmol), and cesium carbonate (0.228 g, 0.7 mmol) in toluene (5 mL) was treated with 2,2,2-trifluoro ethanol (0.082 μL, 0.8 mmol) and stirred at 110° C. for 12 h. After this time the solvent was evaporated and silica gel column chromatography using, typically 30% ethyl acetate in hexane, afforded the desired product (0.110 g, 64%). 1H NMR (300 MHz, CDCl3): δ (ppm) 4.02 (s, 2H), 4.53 (m, 4H), 6.86 (s, 1H), 6.91 (s, 1H), 6.93 (d, 2H), 7.37 (d, 2H). GC-MS: m/z 435 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968570B2
Source datasetuspto-grants-2011_06
ORD IDord-b297efe9ff704657a9eaf132db0d9315
Source noteuspto-grants-2011_06