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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 5-Ethyl-2-methylpyridine | HCID 7728 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 5-Chloro-2-hydroxybenzamide | HCID 348094 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Butyl Acetate | HCID 31272 | — |
| Product | 6-Chloro-2h-1,3-benzoxazine-2,4(3h)-dione | HCID 90359 | 93% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461385B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-8e70ce4c6a0e4055bbc271a7f078c33a |
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| Source note | uspto-grants-2013_06 |
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