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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826714Generated: October 27, 2026

Water → 4-Thiazol-2-yl-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/1826714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridiniumtribromideHCID 21124087—
Reactant4-thiazol-2-yl-1H-indoleHCID 22135413—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Solventtert-ButanolHCID 6386—
Product4-Thiazol-2-yl-1,3-dihydroindol-2-oneHCID 22135439—

Reaction Steps

Pyridinium tribromide (90% (Aldrich), 1.9 g, 5.34 mmol) was added portion-wise over 10 minutes to a suspension of 4-thiazol-2-yl-1H-indole (360 mg, 1.78 mmol) in 2-methyl-2-propanol (15 mL), ethanol (9 mL) and acetic acid (5 mL). The mixture was stirred at room temperature for 2 hours after which acetic acid (18 mL), water (1 mL) and zinc dust (1.5 g, 23.14 mmol) were added. Stirring was continued for 1.5 hours. Residual zinc dust was removed by filtration and washed with methanol. The filtrate was concentrated and the syrupy residue was stirred in water (50 mL) overnight. The solid which formed was filtered, washed with water to remove the zinc and pyridine salts and dried under high vacuum to give 4-thiazol-2-yl-1,3-dihydroindol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053086B2
Source datasetuspto-grants-2006_05
ORD IDord-c374d96abeb9498a8705c217a23d055f
Source noteuspto-grants-2006_05