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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164339Generated: October 30, 2026

Acetic Acid → Methyl 3-hydroxy-5-methoxy-1-phenyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/2164339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 13220377HCID 13220377—
SolventMethanolHCID 887—
ProductMethyl 3-hydroxy-5-methoxy-1-phenyl-1H-indole-2-carboxylateHCID 5469610082%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 1.7 kg (5.2 mole) of 5-methoxy-2-[(2-methoxy-2-oxoethyl)phenylamino]benzoic acid methyl ester, and 303 g (5.6 mole) of sodium methoxide in 10.0 l of anhydrous methanol was stirred at reflux for 90 minutes. The mixture was cooled to 20° C., filtered, and treated with 336 g (320 ml, 5.6 mole) of glacial acetic acid. The mixture was cooled in ice, and the precipitated crude product was filtered and washed with cold methanol followed by hexane. There was obtained 1267 g (82% yield) of the indole product of analytical purity, mp 114°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04503236
Source datasetuspto-grants-1985_03
ORD IDord-4416b813024e403ab708189c04a6a9a8
Source noteuspto-grants-1985_03