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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15268Erstellt: 26. Oktober 2026

Water → 5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dione

https://huagongshe.com/reaction/15268

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt4-Methyloxybenzyl chlorideHCID 69993—
Edukt5-FluoroisatinHCID 236566—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produkt5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dioneHCID 767710080%

Reaktionsschritte

5-Fluoro-1H-indole-2,3-dione (956 mg, 5.79 mmol, 1 eq) was added as a solution in dry DMF to a stirred slurry of sodium hydride (278 mg, 11.6 mmol, 2 eq) in dry DMF drop wise over 15 minutes under an inert atmosphere with adequate pressure release to accommodate H2 evolution. The resulting mixture was stirred for 1 hour and p-methoxybenzyl chloride was added via syringe to the reaction. The solution was then stirred ca 2 hours and worked up by addition of water followed by extraction into ethyl acetate. The organic layer was washed twice with water and then dried over MgSO4. Column chromatography with ethyl acetate/hexane afforded 5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione as a red solid (1.3 g, 80% yield). 1H NMR (CDCl3) δ (ppm): 7.3-7.24 (m, 3H), 7.20 (td, J=8.7, 2.7 Hz, 1H), 6.9-6.86 (m, 2H), 6.76 (dd, J=8.6, 3.6 Hz, 1H), 3.81 (s, 2H), 3.78 (s, 3H). LC/MS=286.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732449B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-dbc008b6d4344431a0479a5e6a29980f
Quellennotizuspto-grants-2010_06