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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26160Generated: October 30, 2026

Ethyl 4,5-dihydro-4-oxo-5-phenylpyrano[3,2-b]indole-2-carboxylate → 4,5-Dihydro-4-oxo-5-phenylpyrano[3,2-b]indole-2-carboxylic acid

https://huagongshe.com/reaction/26160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4,5-dihydro-4-oxo-5-phenylpyrano[3,2-b]indole-2-carboxylateHCID 12628412—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
Product4,5-Dihydro-4-oxo-5-phenylpyrano[3,2-b]indole-2-carboxylic acidHCID 12628429—

Reaction Steps

A mixture of 1.0 g (0.0033 mole) of ethyl 4,5-dihydro-4-oxo-5-phenylpyrano [3,2-b]indole-2-carboxylate in 10 ml glacial acetic acid and 2.0 ml conc. hydrochloric acid was stirred at reflux for 41/2 hr, then cooled and added to 75 g ice - H2O. The solid was filtered, washed with cold water, then added to a mixture of 35 ml 5% aqueous sodium carbonate and 250 ml water. After filtering by gravity, tha aqueous solution was washed three times with 75 ml chloroform, cooled in ice, and acidified with 4.0 N hydrochloric acid. The orange precipitate was filtered, digested 15 min on the steam bath with 25 ml water and re-filtered warm. Recrystallization from DMF-water yielded an off-white solid of mpt.>290°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04148806
Source datasetuspto-grants-1979_04
ORD IDord-0a202b9cede1473991f009021cb0bc23
Source noteuspto-grants-1979_04