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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853831Generated: October 27, 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/853831

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, J=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 numberUS07256207B2
Source datasetuspto-grants-2007_08
ORD IDord-615616959e0c4b5aa6b645206817e24b
Source noteuspto-grants-2007_08