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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266982Generated: October 31, 2026

2-Amino-3-chlorobenzoic acid → 8-chloro-3,4-dihydro-2H-1-oxa-4a,9-diaza-anthracen-10-one

https://huagongshe.com/reaction/1266982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-chlorobenzoic acidHCID 80807—
ReactantPropane, 1-chloro-3-isocyanato-HCID 166752—
SolventWaterHCID 962—
Product8-chloro-3,4-dihydro-2H-1-oxa-4a,9-diaza-anthracen-10-oneHCID 1145902682.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 250 mL round bottom flask is charged with 2-amino-3-chlorobenzoic acid (5.00 g, 29.1 mmol) and 40 mL of 10% aqueous KHCO3. The slurry is cooled to 0° C., and 3-chloropropylisocyanate (5.25 mL, 51.2 mmol) is added. The reaction mixture is allowed to warm to room temperature over 3 hours, warmed to reflux for 2 hours, then stirred at room temperature for 16 hours. It is then diluted with 40 mL H2O and cooled to 0° C. The product is collected by filtration to provide 5.68 g of a yellow solid. This material is purified by recrystallization: it is dissolved in a minimal volume of warm CH2Cl2 (ca. 10 mL), cooled to 0° C., and IPE (ca. 20 mL) added to the point of cloudiness; crystallization is allowed to proceed at that temperature for 1 hour. The resulting yellow solid is collected and dried to provide 3.87 g (16.3 mmol, 56% yield) of light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552015B2
Source datasetuspto-grants-2003_04
ORD IDord-b3bf17194a18463c850b5a7b9bd6fe62
Source noteuspto-grants-2003_04