Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370642Generated: November 3, 2026

Oxalyl chloride → HCID 10684544, compound

https://huagongshe.com/reaction/1370642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 10851968HCID 10851968—
SolventDichloromethaneHCID 6344—
ProductHCID 10684544HCID 1068454496.6%

Reaction Steps

A solution of 3-(4-tert-butylbenzoyl)amino-2-thiophenecarboxylic acid (8.1 g, 27 mmol) in methylene chloride (135 mL) was treated with oxalyl chloride (11.8 mL, 135 mmol). The mixture was slowly heated to afford a homogeneous solution. After 2 h, the mixture was concentrated in vacuo and the residue dissolved in methylene chloride (135 mL) and treated with pyridine (2.2 mL). After 1 hr, the mixture was concentrated in vacuo and the residue partitioned between ethyl acetate and water. The organic layer was washed four times with water, once with saturated sodium chloride solution, dried (magnesium sulfate), and filtered. Concentration and purification of the residue by flash chromatography (silica gel, hexanes/ethyl acetate) yielded 7.44 g (96%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583173B2
Source datasetuspto-grants-2003_06
ORD IDord-21cddbae942442a7bd8ff390fa03575e
Source noteuspto-grants-2003_06