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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871473Generated: November 2, 2026

Acetaldehyde → HCID 15462583, compound

https://huagongshe.com/reaction/1871473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18691101HCID 18691101—
SolventEthanolHCID 702—
ProductHCID 15462583HCID 15462583—

Reaction Steps

To a solution of 5.0 g of 3-amino-9-methoxy-2-(2-methylphenyl)imidazo[2,1-a]isoquinoline (Compound 26) in 100 ml of ethanol was added 3.0 ml of acetaldehyde, and the mixture was stirred at room temperature for 3 hours. After 3.3 g of sodium borohydride was added to the mixture and refluxed for 2 hours, the reaction mixture was poured into water, and extracted with ethyl acetate. The extract was washed with saturated saline, and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was removed under reduced pressure. The crude crystal was recrystallized from petroleum ether/ethyl acetate to give 5.0 g of the title compound as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06103736
Source datasetuspto-grants-2000_08
ORD IDord-e861ed950a5947f1aaf181c85df0af44
Source noteuspto-grants-2000_08