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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107958Generated: November 2, 2026

Water → 1-Acetyl-3-(2-carboxyethyl)-4,6-dimethylindoline

https://huagongshe.com/reaction/1107958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Acetyl-3-(2-cyanoethyl)-4,6-dimethylindolineHCID 22247304—
SolventEthanolHCID 702—
Product1-Acetyl-3-(2-carboxyethyl)-4,6-dimethylindolineHCID 22247345—

Reaction Steps

1-Acetyl-3-(2-cyanoethyl)-4,6-dimethylindoline (4.5 g) was dissolved in EtOH (150 ml), and a solution of KOH (10.4 g) in water (50 ml) was added, which was followed by refluxing for 15 hr. EtOH was evaporated under reduced pressure, and the aqueous layer was adjusted to weak acidic with 6N hydrochloric acid and extracted with CHCl3 (100 ml). The CHCl3 layer was washed with water and dried over anhydrous sodium sulfate. CHCl3 was evaporated under reduced pressure. The residue was dissolved in CHCl3 (20 ml) and Ac2O (1.9 g) was added, which was followed by stirring at room temperature for 1 hr. CHCl3 (100 ml) was added, and the mixture was washed with water and dried over anhydrous sodium sulfate. CHCl3 was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: CHCl3 /MeOH=50/1-10/1) to give 3.4 g of 1-acetyl-3-(2-carboxyethyl)-4,6-dimethylindoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063806
Source datasetuspto-grants-2000_05
ORD IDord-4fedcb92ca144c1b8248486b48a8512f
Source noteuspto-grants-2000_05