Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846313Generated: October 31, 2026

Pyridine → 3-Chloroisatoic anhydride

https://huagongshe.com/reaction/1846313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Amino-3-chlorobenzoic acidHCID 80807—
ReactantTriphosgeneHCID 94429—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product3-Chloroisatoic anhydrideHCID 517535—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a stirred solution of 2-amino-3-chlorobenzoic acid (0.86 g, 5.00 mmol) in anhydrous acetonitrile (10 mL), a solution of triphosgene (0.49 g, 1.65 mmol) in anhydrous CH2Cl2 (5 mL) and anhydrous pyridine (0.79 g, 10.0 mmol) were added, drop-wise at 55° C., simultaneously over a period of 10 minutes. After the addition was complete, the reaction mixture was stirred at 55° C. for another 2 hours. The solvents were removed under vacuum and water (50 mL) was added. The separated solid was filtered, washed with water, followed by chilled CH2Cl2 (10 mL) and dried under vacuum to give 8-chloro-1H-benzo[d][1,3]oxazine-2,4-dione as an off-white solid. Yield 0.82 g (83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952021B2
Source datasetuspto-grants-2015_02
ORD IDord-2c2607b800a94fb1a6929920e970d4d2
Source noteuspto-grants-2015_02