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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012568Generated: November 1, 2026

Formic Acid → 4-[(4-Dipropylaminobutyl)methylamino]methylbenzonitrile

https://huagongshe.com/reaction/1012568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15965417HCID 15965417—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-[(4-Dipropylaminobutyl)methylamino]methylbenzonitrileHCID 1611729395%

Reaction Steps

16 g (56 mmol, 1.0 equivalent) of 4-[(4-dipropylaminobutyl)amino]methylbenzonitrile (2a), 50 ml of ethanol, 11.9 g (139 mmol, 2.5 equivalents) of a formaldehyde aqueous solution (35%), and 12.8 g (278 mmol, 5 equivalents) of formic acid were charged in a 300 ml four-necked flask. The mixture was reacted at 80° C. for one hour. The raw material was then disappeared. The reaction solution was slowly added to a solution prepared by dissolving 40 g of sodium hydroxide in 200 ml of distilled water. The reaction solution was extracted with 200 ml of chloroform. This operation was repeated twice. The chloroform layer was then dried over anhydrous sodium sulfate. The solvent was then concentrated, thereby obtaining 16 g of 4-[(4-dipropylaminobutyl)methylamino]methylbenzonitrile (2b) as a slightly yellow oily substance (yield: 95%). [HPLC: 99% (HPLC measurement conditions A)]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977512B2
Source datasetuspto-grants-2011_07
ORD IDord-9b6db48853654b048cf26f8eaed865f0
Source noteuspto-grants-2011_07