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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246285Generated: October 25, 2026

Acetonitrile → 4-(Dimethylamino)-2-butenoyl chloride hydrochloride

https://huagongshe.com/reaction/1246285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantDimethyl oxalateHCID 11120—
ReactantOxalyl chlorideHCID 65578—
Reactant(2E)-4-(Dimethylamino)-2-butenoic acid hydrochlorideHCID 45358758—
SolventDimethylformamideHCID 6228—
Product4-(Dimethylamino)-2-butenoyl chloride hydrochlorideHCID 73853253—

Reaction Steps

A 1 L multi-neck flask equipped with agitator, thermometer, addition funnel, and nitrogen protection is charged with acetonitrile (0.67 kg, 0.85 L) followed by adding dimethylformamide (0.00086 kg, 0.91 mL, d=0.944 g/mL). At ambient temperature, is added 4-dimethylaminocrotonic acid hydrochloride (0.0709 kg) and the mixture stirred until homogeneous. Cool the reaction mixture to (0–10° C.) and add oxalyl chloride (0.0473 kg, 0.0325 L, d=1.45 g/mL) dropwise over (20 minutes) at (0–10° C.) followed by a rinse with acetonitrile (0.02 kg, 0.03 L). The temperature (0–10° C.) is maintained for about (20 minutes). The temperature of the reaction mixture is adjusted to (22–26° C.) over (20 minutes) and maintained over (2 hours). The temperature of reaction mixture is adjusted to (40–45° C.) and held for about (5 minutes). Cool the light suspension to about (20–25° C.) and check for reaction completion by high-pressure liquid chromatography (HPLC). The reaction is complete when there is ≦15% of the starting material (4-dimethylaminocrotonic acid hydrochloride) present and/or ≦2% of oxalyl chloride (detected as the dimethyl oxalate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07126025B2
Source datasetuspto-grants-2006_10
ORD IDord-74ac10285c504dd6b77f3cf8821bc883
Source noteuspto-grants-2006_10