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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191411Generated: November 3, 2026

Acetic Acid → 4-(2,3-Difluoro-phenyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2191411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-ButanolHCID 6386—
ReactantPyridiniumtribromideHCID 21124087—
ReactantHCID 22561761HCID 22561761—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
Product4-(2,3-Difluoro-phenyl)-1,3-dihydro-indol-2-oneHCID 2256197197%

Reaction Steps

4-(2,3-difluoro-phenyl)-1H-indole 6c (744 mg, 3.25 mmol) was dissolved in 12 ml of ethanol under stirring, and added successively with tert-butanol (21 ml), glacial acetic acid (6.4 ml) and pyridinium tribromide (3.12 g, 9.7 mmol) at room temperature. Upon completion of the addition, the reaction mixture was stirred for 3 hours, added with glacial acetic acid (16 ml) and zinc dust (1.1 g, 16.25 mmol), and stirred for another 1 hour. The reaction mixture was filtered and concentrated under reduced pressure. The residue was added with ethyl acetate (30 ml), washed successively with water (10 ml), saturated sodium bicarbonate solution (10 ml) and saturated brine (10 ml), dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure to obtain 4-(2,3-difluoro-phenyl)-1,3-dihydro-indol-2-one 6d (780 mg, yield 97%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329682B2
Source datasetuspto-grants-2012_12
ORD IDord-6b99baa547f94c3798ae719d931084f7
Source noteuspto-grants-2012_12