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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598176Generated: October 25, 2026

Acetic Anhydride → (E)-2-(2,6-dichlorobenzoyl)-3-(1-propylbutylamino)acrylonitrile

https://huagongshe.com/reaction/598176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
Reactant4-HeptanamineHCID 38665—
Reactant3-(2,6-Dichlorophenyl)-3-oxopropiononitrileHCID 3018140—
SolventTetrahydrofuranHCID 8028—
Product(E)-2-(2,6-dichlorobenzoyl)-3-(1-propylbutylamino)acrylonitrileHCID 6726733910.5%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 3-(2,6-dichlorophenyl)-3-oxopropanenitrile (0.200 g, 0.93 mmol), acetic anhydride (0.22 g, 2.20 mmol), and triethyl orthoformate (0.21 g, 1.40 mmol) was stirred at 150° C. for 1 hr. The solution was then concentrated and the residue redissolved in ethanol (5 mL). 4-heptylamine (0.16 g, 1.4 mmol) in 1 mL of tetrahydrofuran was added to the reaction mixture at 0° C. The reaction stirred for 30 minutes and was then concentrated. Flash chromatography (20% Ethyl acetate/hexanes) gave the desired compound (0.033 g, 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897607B2
Source datasetuspto-grants-2011_03
ORD IDord-c02c2c1bc69342f3afc648452bc0ea63
Source noteuspto-grants-2011_03