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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110036Generated: November 2, 2026

Oxalyl chloride → 5-Chloroisatoic anhydride

https://huagongshe.com/reaction/2110036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-[(tert-Butoxycarbonyl)amino]-6-chlorobenzoic acidHCID 17750447—
SolventTolueneHCID 1140—
Product5-Chloroisatoic anhydrideHCID 78480—

Reaction Steps

After suspending 2-(Boc)amino-6-chlorobenzoic acid (1.51 g, 5.56 mmol) in toluene (20 mL), the mixture was heated to reflux. Oxalyl chloride (0.572 mL, 6.67 mmol) was added dropwise thereto, and the mixture was vigorously stirred for 10 minutes. After cooling the reaction mixture on ice, the precipitated crystals were filtered out, washed with n-hexane and dried in a desiccator to obtain 5-chloroisatoic anhydride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517875B2
Source datasetuspto-grants-2009_04
ORD IDord-f70b25d3c94f4b0ea9b6af9c6d3fc4b9
Source noteuspto-grants-2009_04