HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19443Erstellt: 23. Oktober 2026
Hydrochloric Acid → 6-Chloro-2h-1,3-benzoxazine-2,4(3h)-dione
https://huagongshe.com/de/reaction/19443
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | 5-Chloro-2-hydroxybenzamide | HCID 348094 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 6-Chloro-2h-1,3-benzoxazine-2,4(3h)-dione | HCID 90359 | 85,3% |
Reaktionsschritte
A solution of 10 g of 5-chloro-2-hydroxybenzamide (58.0 mmol), pyridine (22 ml) and acetonitrile (25 ml) was stirred in an ice bath. Ethyl chloroformate (6.1 ml, 0.0638 mol) was added dropwise. The pink solution was stirred for 30 minutes at <10° C. The ice bath was replaced with an oil bath. The reaction mixture was heated to 95° C. and the volatiles were distilled off (43 ml). The reaction was cooled to room temperature, causing a white solid to form. The mixture was poured into water (100 ml) and acidified with concentrated aqueous hydrochloric acid. The resulting solid was filtered and recrystallized in hot ethanol to give 9.77 g of 6-chloro-2H-1,3-benzoxazine-2,4(3H)-dione.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07744910B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-d1b5b65db5a349c791c13059ce7ef66b |
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| Quellennotiz | uspto-grants-2010_06 |
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