Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459756Generated: October 26, 2026

Ammonium Chloride → 3-(3-amino-4-fluorobenzylidene)-3H-isobenzofuran-1-one

https://huagongshe.com/reaction/459756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-oneHCID 68624589—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product3-(3-amino-4-fluorobenzylidene)-3H-isobenzofuran-1-oneHCID 68622747—

Reaction Conditions

Temperature70 °C

Reaction Steps

A stirred mixture of the above crude 3-(4-fluoro-3nitrobenzylidene)-3H-isobenzofuran-1-one (23.5 g), industrial methylated spirit (400 ml), water (300 ml) and ammonium chloride (8.81 g, 0.165 mol) was heated to 70° C., and iron powder (46.0 g, 0.824 gatom) was added in portions. When the addition was complete, the stirred mixture was heated at 70° C. for a further 2 hours, then it was filtered while hot through Celite. The collected inorganic solids were washed with hot industrial methylated spirit (6×200 ml), then the filtrate and washings were combined and the solvent was removed in vacuo. The residue was triturated with water (300 ml) and the resulting solid was collected by filtration and dried in vacuo for 24 hours to give crude 3-(3-amino-4-fluorobenzylidene)-3H-isobenzofuran-1-one as a yellow solid, m/z (M+H)+. 256, 100% purity, which was used directly in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196085B2
Source datasetuspto-grants-2007_03
ORD IDord-395bd31dc99b41bf942731b9f00a0db7
Source noteuspto-grants-2007_03