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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4023Generated: October 26, 2026

Ethylene Glycol → 2-(5-Methyl-7-nitro-1-indolinyl)benzoic acid

https://huagongshe.com/reaction/4023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantDichloromethaneHCID 6344—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(5-Methyl-7-nitroindolin-1-yl)benzonitrileHCID 13823337—
SolventWaterHCID 962—
Product2-(5-Methyl-7-nitro-1-indolinyl)benzoic acidHCID 1402368032%

Reaction Conditions

Temperature175 °C

Reaction Steps

A stirred solution under nitrogen of potassium hydroxide (30 g, 0.53 mole) in ethylene glycol (250 ml) and water (35 ml) was heated to 175° C., at which temperature there was added 2-(5-methyl-7-nitroindolin-1-yl)benzonitrile (26 g, 0.093 mole). After heating at 175° C. for 3 hours, the reaction mixture was cooled to room temperature and dichloromethane (1 liter) and water (500 ml), were added, with stirring. The aqueous phase was separated and extracted with two 250 ml-portions of dichloromethane. The aqueous phase was then cooled in an ice-bath and acidified with concentrated hydrochloric acid. The product was extracted out with three 500 ml-portions of dichloromethane. The combined organic extracts were washed twice with brine, dried, filtered, and concentrated to afford 9.0 g (32%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723007
Source datasetuspto-grants-1988_02
ORD IDord-c00a9480d9f0457d8175dcbd5a9b8e1d
Source noteuspto-grants-1988_02