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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914605Generated: November 3, 2026

Thionyl Chloride → HCID 59293381, compound

https://huagongshe.com/reaction/1914605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2,5-dichloropyridine-4-carboxylic 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 numberUS08614212B2
Source datasetuspto-grants-2013_12
ORD IDord-c89714c905be47429d7db29b402245a6
Source noteuspto-grants-2013_12