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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725965Generated: October 30, 2026

Ethanol → HCID 21842736, compound

https://huagongshe.com/reaction/725965

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 21842736HCID 2184273642%

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 numberUS05708008
Source datasetuspto-grants-1998_01
ORD IDord-9bd6ddf93a7e4ef3bf41fc0fe273f9c4
Source noteuspto-grants-1998_01