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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893266Generated: October 26, 2026

Acetic Acid → Dimethylaminomethylbenzylcyanide

https://huagongshe.com/reaction/893266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-ButanolHCID 263—
ReactantDimethylamineHCID 674—
ReactantWaterHCID 962—
Reactant2-(4-(Bromomethyl)phenyl)acetonitrileHCID 14342076—
SolventMethanolHCID 887—
ProductDimethylaminomethylbenzylcyanideHCID 415903—

Reaction Steps

In a 1 liter round bottomed flask with condenser and thermometer 8.2 g of 4-bromomethylbenzylcyanide are dissolved in 453 ml methanol and cooled to +3° C. At this temperature 12.7 ml of 40% dimethylamine solution are added drop-by-drop. The solution is subsequently stirred for 1/4 hour at +5° C. and 2 hours at room temperature. The reaction sequence is controlled by means of thin-layer chromatography (0.57 ml of specimen+0.43 ml methanol: eluent n-butanol: acetic acid: water=4:1:1; v/v; 10 μl coating; HPTLC finished plated diatomaceous earth 60 F 254). Following removal of the volatile components is a rotary evaporator (20 torr, 40° C. bath temperature) the residue is absorbed in 20 ml 1N hydrochloric acid and extracted with a total of 150 ml of diethyl ether. The clear, aqueous phase is treated with 30 ml of 1N sodium hydroxide solution (ice cold) and extracted subsequently with 250 ml of diethyl ether. The organic phase is washed to neutrality with a saturated solution of common salt, dried with sodium sulfate and evaporated to dryness in a rotary evaporator (30° C. bath temperature, 20 torr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05124326
Source datasetuspto-grants-1992_06
ORD IDord-370b8ce48f7f48c3bafaecdb5121d806
Source noteuspto-grants-1992_06