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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708588Generated: October 30, 2026

Dimethylformamide → HCID 86748203, compound

https://huagongshe.com/reaction/1708588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalic acid dihydrateHCID 61373—
ReactantOxalyl chlorideHCID 65578—
Reactant3-DimethylaminoacrylonitrileHCID 5324735—
Solvent1,2-DichloroethaneHCID 11—
SolventIsopropanolHCID 3776—
ProductHCID 86748203HCID 8674820397.2%

Reaction Steps

A solution of oxalyl chloride (13.1 mL, 0.15 mol) in 1,2-dichloroethane is added dropwise to a solution of N,N-dimethylformamide (11.6 mL, 0.15 mol) in 1,2-dichloroethane while maintaining the reaction mixture temperature below 0° C. The reaction mixture is stirred for 45 minutes, treated with a solution of trans-3-dimethylaminoacrylonitrile (16.4 mL, 0.15 mol) in 1,2-dichloroethane, stirred at room temperature for 16 hours, refluxed for two hours and concentrated in vacuo to obtain a semi-solid residue. A solution of the residue in 2-propanol is treated with a solution of oxalic acid dihydrate (18.9 g, 0.15 mol) in 2-propanol and warmed until a clear solution is obtained. The clear solution is cooled to and held at room temperature for several hours, cooled in a freezer for two hours and filtered. The filter cake is washed sequentially with 2-propanol and ether and dried in a vacuum desiccator at 50° to give the title product (28.6 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359089
Source datasetuspto-grants-1994_10
ORD IDord-bf78782cf64f4be3bbe81445ac34a6ae
Source noteuspto-grants-1994_10