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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292709Generated: October 30, 2026

Acetaldehyde → HCID 19788471, compound

https://huagongshe.com/reaction/1292709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
Reactant4-MethylbenzenethiolHCID 7811—
Reactant5-AminoquinolineHCID 11911—
SolventEthanolHCID 702—
ProductHCID 19788471HCID 1978847162.7%

Reaction Steps

A mixture of 5-aminoquinoline (7.2 g, 0.05 mol), acetaldehyde (2.6 g, 0.06 mol) and 4-thiocresol (6.8 g, 0.055 mol) in ethanol (100 ml) was stirred at reflux for 4 h. The reaction mixture was evaporated under reduced pressure and the residue dissolved in ethanol (100 ml). Sodium borohydride (10 g) was then added to the reaction mixture in portions maintaining the temperature below 5° C. This reaction mixture was stirred at reflux for 2 h and cooled to room temperature. Water (40 ml) was then added and the mixture was stirred for a further 25 min at reflux. The pH of the mixture was then adjusted to pH8 with 2N NaOH and the product was extracted with dichloromethane (4×100 ml). The dichloromethane extracts were combined and washed with water (250 ml) before being dried over MgSO4. The solvent was then removed under reduced pressure and the residue was purified by column chromatography on silica gel eluting with ethyl acetate in hexane. The solvent in the eluent was evaporated to give 5.4 g of a yellow solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238228B2
Source datasetuspto-grants-2007_07
ORD IDord-c372c28b576d4985b19070cbe4df72b0
Source noteuspto-grants-2007_07