HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27972Erstellt: 23. Oktober 2026
Hydrochloric Acid → 4H-1,3-Benzoxazin-4-one, 6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-
https://huagongshe.com/de/reaction/27972
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Benzamide, 5-chloro-N,2-dihydroxy- | HCID 169935 | — |
| Edukt | Crotonaldehyde | HCID 447466 | — |
| Edukt | 6-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one | HCID 12365927 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 4H-1,3-Benzoxazin-4-one, 6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy- | HCID 112684 | — |
Reaktionsschritte
Prior to the present invention, 6-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one has been prepared by the reaction of 5-chlorosalicylhydroxamic acid (made from 5-chlorosalicylate and hydroxylamine) and crotonaldehyde in the presence of hydrogen chloride and glacial acetic acid to obtain 6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-4H-1,3-benzoxazin-4-one. The latter compound was then cyclized to 7-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one. Said cyclization can be carried out using organic or inorganic bases in the appropriate solvent. U.S. Pat. No. 3,598,814 discloses and claims 7-chloro-2-methyl-3, 3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one and several methods for its manufacture.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04224443 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-f831b10a89984c7a966ec6bbcd621d7c |
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| Quellennotiz | uspto-grants-1980_09 |
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