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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043321Generated: October 28, 2026

N-Ethylaniline → HCID 24946957, compound

https://huagongshe.com/reaction/2043321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-EthylanilineHCID 7670—
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
CatalystAcetic AcidHCID 176—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
ProductHCID 24946957HCID 2494695751%

Reaction Steps

To a solution of N-ethylaniline (0.145 g, 1.2 mmol) in 1,2-dichloroethane (5 ml) were added molecular sieves (2 g, size 0.4 nM) and 4-formylimidazole (0.3 g, 3.12 mmol). After stirring the mixture for 5 min at room temperature sodium triacetoxyborohydride (1.02 g, 4.8 mmol) and acetic acid (5 drops) were added. The reaction mixture was stirred at room temperature overnight. For workup ethyl acetate (50 ml) and 1 M sodium bicarbonate solution (30 ml) were added and the mixture was shaken. The organic layer was separated, dried over magnesium sulfate and evaporated. The residue was purified using flash chromatography (column: Isolute® Flash-NH2 (Separtis); eluent: ethyl acetate/methanol=95:5) to yield a white solid (122 mg, 51%); MS (ISP): 202.0 ((M+H)+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586617B2
Source datasetuspto-grants-2013_11
ORD IDord-3612db451a304aa6bcc12d2fc33ead98
Source noteuspto-grants-2013_11