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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257486Generated: October 31, 2026

Hydrochloric Acid → 6-Chloro-2h-1,3-benzoxazine-2,4(3h)-dione

https://huagongshe.com/reaction/1257486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Ethyl-2-methylpyridineHCID 7728—
ReactantEthyl chloroformateHCID 10928—
Reactant5-Chloro-2-hydroxybenzamideHCID 348094—
SolventWaterHCID 962—
SolventButyl AcetateHCID 31272—
Product6-Chloro-2h-1,3-benzoxazine-2,4(3h)-dioneHCID 9035993%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

5-chlorosalicylamide (300 g, 1.75 mol) and water (900 ml) were placed in a 3 liter, 4-neck round-bottomed flask under a nitrogen atmosphere and stirred. 5-ethyl-2-methyl-pyridine (284 g, 2.27 mol) and n-butyl acetate (900 ml) were added to the mixture. The mixture was cooled to 0-5° C. (jacket-10° C.) and dropwise addition of ethyl chloroformate (233 g, 2.10 mol) was started. This addition continued over a period of approximately one hour. When the addition was completed, the reaction mixture was slowly heated (in about two hours) to reflux and kept under reflux for an additional period of about 5 hours (jacket 110° C., internal temperature (IT) 90° C.). The resulting slurry was allowed to cool to room temperature, and hydrochloric acid (28 ml, 37% m/m, 0.34 mol) was added and the mixture stirred for about 30 minutes. The resulting slurry was vacuum filtered, the filter cake was washed with n-butyl acetate followed by water (600 ml) and was allowed to dry overnight in vacuo at 60° C. 321 g (93%) of 6-chloro-2H-1,3-benzoxazine-2,4(3H)-dione (6-chloro carsalam) was isolated after drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461385B2
Source datasetuspto-grants-2013_06
ORD IDord-8e70ce4c6a0e4055bbc271a7f078c33a
Source noteuspto-grants-2013_06