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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164335Generated: October 31, 2026

Water → 3-Methoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxylic acid

https://huagongshe.com/reaction/2164335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13220385HCID 13220385—
SolventMethanolHCID 887—
Product3-Methoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxylic acidHCID 1322039445%

Reaction Steps

A suspension of 13.5 g (0.042 mole) of 3-methoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxylic acid methyl ester in 75 ml of methanol was treated with 70.6 ml of 1.0N aqueous sodium hydroxide. The mixture was stirred at reflux for 17 hours, then added to 1.4 l of water. The insoluble material was filtered, added to 1.0 l of water, and acidified with acetic acid while cooling in an ice bath. The crude acid product was recovered by filtration. The original filtrate from the reaction mixture and 1.4 l of water was also cooled in ice and acidified with acetic acid. The crude product obtained was filtered and combined with the earlier crop. The combined crude products were stirred in 400 ml of water, filtered, and recrystallized from methanol. There are obtained 5.8 g (45% yield) of analytically pure acid, mp 154°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04503236
Source datasetuspto-grants-1985_03
ORD IDord-ff75efe93967467383a97ed42f11bd65
Source noteuspto-grants-1985_03