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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731743Generated: November 3, 2026

Acetic Acid → HCID 13505189, compound

https://huagongshe.com/reaction/1731743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 13505188HCID 13505188—
SolventEthanolHCID 702—
ProductHCID 13505189HCID 1350518994.2%

Reaction Steps

440 mg (1.31 mmol) of 6-(1-cyclohexen-4-yl)-4-methyl-β-carboline-3-carboxylic acid ethyl ester is heated under reflux for one hour in 20 ml of ethanol with 3.25 ml of 1N potassium hydroxide solution. After neutralizing with acetic acid and addition of 10 ml of water, the precipitated product is suctioned off, washed with water, and dried under vacuum over potassium hydroxide, thus obtaining 378 mg (94% of theory) of 6-(1-cyclohexen-4-yl)-4-methyl-β-carboline-3-carboxylic acid, mp 284°-285° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623649
Source datasetuspto-grants-1986_11
ORD IDord-c40bd39e5f304e06876035e8c71181da
Source noteuspto-grants-1986_11