Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038460Generated: October 31, 2026

Thionyl Chloride → HCID 59293381, compound

https://huagongshe.com/reaction/1038460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2,5-Dichloroisonicotinic acidHCID 2736087—
ReactantPotassium ethyl malonateHCID 3446434—
ReactantMagnesium ChlorideHCID 5360315—
CatalystDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 59293381HCID 59293381—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 2,5-dichloropyridine-4-carboxylic acid (2 g) and SOCl2 (10 ml) and 1 drop of DMF were heated under reflux for 2 h, and all SOCl2 and DMF removed under reduced pressure to give the crude acid chloride as the remaining residue. Separately, a suspension of potassium ethyl malonate (5 g) in acetonitrile (100 ml) was cooled to 0° C., magnesium chloride (4 g) and triethylamine (4 ml) were added, the ice bath removed and the reaction stirred at RT for 3 h. A solution of the crude acid chloride in DCM (25 ml) was carefully added to the malonate slurry and the resulting mixture stirred at RT overnight. Aqueous HCl (100 ml, 1M) was added and stiffing continued for 1 h. This mixture was then extracted with diethyl ether (200 ml×3), the organic layer washed with saturated sodium bicarbonate (200 ml×2) and brine (200 ml), dried over anhydrous magnesium sulfate, filtered and concentrated. The title compound was obtained as light yellow oil (1.6 g) which was on-reacted without further purification and without further characterization other than ascertaining that the compound was one spot by tlc with the expected molecular weight (M−1) of 260.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551990B2
Source datasetuspto-grants-2013_10
ORD IDord-1d0a8af038b64ab78d8f9ed12221bced
Source noteuspto-grants-2013_10