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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012578Generated: November 1, 2026

4-(Diethylamino)benzaldehyde → HCID 16117295, compound

https://huagongshe.com/reaction/1012578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Diethylamino)benzaldehydeHCID 67114—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 15965417HCID 15965417—
SolventEthanolHCID 702—
ProductHCID 16117295HCID 1611729534.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.473 g (1.65 mmol) of 4-[(4-dipropylaminobutyl)amino]methylbenzonitrile (2a), 9.5 ml of ethanol, and 583 mg (3.29 mmol, 2.0 equivalents) of 4-diethylaminobenzaldehyde were charged in a 50 ml recovery flask under a nitrogen stream. The mixture was then cooled to 0° C. After the addition of 0.837 g (3.95 mmol, 2.4 equivalents) of sodium triacetoxyborohydride, the mixture was stirred at room temperature for 17 hours. After confirming the disappearance of the raw material by TLC, the reaction solution was added to 50 ml of a saturated sodium bicarbonate aqueous solution, and was extracted twice with 50 ml of chloroform. The chloroform layer was washed with 100 ml of a saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate, concentrated, and purified by silica gel column chromatography (Chromatorex NH, chloroform:n-hexane=1:1), thereby obtaining 0.252 g of 4-{[(4-diethylaminobenzyl)-(4-dipropylaminobutyl)amino]methyl}benzonitrile (16) as a light yellow oily substance (yield: 34.1%). [HPLC: 98.7% (HPLC measurement conditions B)]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977512B2
Source datasetuspto-grants-2011_07
ORD IDord-cf5dd77c7d744fad828c16420961c869
Source noteuspto-grants-2011_07