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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737716Generated: November 2, 2026

Ethanol → HCID 14973215, compound

https://huagongshe.com/reaction/1737716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole-5-carboxylic acidHCID 19022984—
ProductHCID 14973215HCID 1497321542%

Reaction Steps

A solution of 0.513 gm (2 mMol) 5-carboxy-3-(1-methyl-1,2,5,6-tetrahydropyridin-4-yl)-1H-indole in 5.1 mL ethanol was cooled in an ice bath while 0.51 mL sulfuric acid was added dropwise. The resulting mixture was heated at reflux for 5 hours. The now homogeneous solution was poured into 50 mL cold water and was then made basic with saturated ammonium hydroxide. The light yellow precipitate was collected by filtration and then recrystallized from ethanol to provide 0.24 gm (42%) of the desired compound as light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962474
Source datasetuspto-grants-1999_10
ORD IDord-00cec62b697a4d418bb2c259d31ae262
Source noteuspto-grants-1999_10