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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35127Generated: October 25, 2026

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

https://huagongshe.com/reaction/35127

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 numberUS04764616
Source datasetuspto-grants-1988_08
ORD IDord-ca263d7b81ca4beda3f0ccebf20713ef
Source noteuspto-grants-1988_08