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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249941Generated: October 26, 2026

5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dione → 5-Fluoro-1-(4-methoxy-benzyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2249941

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dioneHCID 7677100—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventHydrazine hydrate (1:1)HCID 24654—
Product5-Fluoro-1-(4-methoxy-benzyl)-1,3-dihydro-indol-2-oneHCID 2108225690.3%

Reaction Steps

A solution of 5-fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione (7.1 g, 24.9 mmol) in hydrazine hydrate (35 mL) and ethanol (15 mL) was refluxed overnight, diluted with water and extracted twice with ethyl acetate. The combined organics were dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography using a gradient of 0-100% ethyl acetate in hexane to afford 6.1 g (90%) of 5-fluoro-1-(4-methoxy-benzyl)-1,3-dihydro-indol-2-one; 1H NMR (CDCl3, 400 MHz) δ 3.59 (s, 2H), 3.77 (s, 3H), 4.83 (s, 2H), 6.63 (dd, 1H, J1=4.2, J2=8.6), 6.82-6.91 (m, 3H), 6.96-7.01 (m, 1H), 7.19-7.23 (m, 1H), 7.27-7.31 (m, 1H); HPLC-MS calcd. for C16H14FNO2 (M+H+) 272.1. found 272.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314872B2
Source datasetuspto-grants-2008_01
ORD IDord-438a2df07585439682976b9c6cbf888e
Source noteuspto-grants-2008_01