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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786437Generated: 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/1786437

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 numberUS07507755B2
Source datasetuspto-grants-2009_03
ORD IDord-16b226f5d2f74826891bc220841267bf
Source noteuspto-grants-2009_03