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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600762Generated: October 29, 2026

Oxalyl chloride → 3-[5-(2-Fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl isocyanate

https://huagongshe.com/reaction/600762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-[5-(2-Fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzamideHCID 44142326—
SolventDichloromethaneHCID 6344—
Product3-[5-(2-Fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl isocyanateHCID 5782251595%

Reaction Conditions

Temperature0 °C

Reaction Steps

Oxalyl chloride (2.5 ml, 28.2 mmol, 2.0 eq.) is then added dropwise under N2 to a suspension of 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzamide (Compound A3, 4.0 g, 14.1 mmol) in anhydrous dichloromethane (20 mL) cooled to 0° C. The mixture is slowly heated to reflux and stirred for an additional 6 h. The solvent is removed on a rotary evaporator. The residue is azeotroped with anhydrous dichloromethane (20 mL) and dried under high vacuum for two hours to give 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl isocyanate (Compound A4) as a tan solid 4.12 g (95%) which may be used immediately without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902235B2
Source datasetuspto-grants-2011_03
ORD IDord-f05b2624b003425e8aecd69d8918fad0
Source noteuspto-grants-2011_03