HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1706779Erstellt: 24. Oktober 2026
Bentazon → 1-(2-chloroacetyl)-3-(1-methylethyl)--1H-2,1,3-benzothiadiazin-4 (3H)-one-2,2-dioxide
https://huagongshe.com/de/reaction/1706779
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Bentazon | HCID 2328 | — |
| Edukt | Chloroacetyl chloride | HCID 6577 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-(2-chloroacetyl)-3-(1-methylethyl)--1H-2,1,3-benzothiadiazin-4 (3H)-one-2,2-dioxide | HCID 20334432 | — |
Reaktionsschritte
To 100 ml of acetonitrile was added 10.0 g of 3-(1-methylethyl)-1H-2,1,3-benzothiadiazin-4(3H)-one- -2,2-dioxide and 4.9 g of potassium t-butoxide. The mixture was stirred vigorously and 3.3 ml of chloroacetyl chloride in 50 ml acetanitrile was added dropwise over a 0.5 hour period. The resultant mixture as stirred overnight, filtered and the solvent removed from the filtrate in vacuo. The residue was washed with carbon tetrachloride and filtered. The tan granular precipitate was dissolved in 50 ml of methylene chloride and 50 ml of carbon tetrachloride was added. The methylene chloride was removed under a nitrogen atmosphere and the resultant mixture was filtered. The precipitate was washed 5% aqueous potassium carbonate, filtered and the white flocculent precipitate air dried to afford 2.23 g of 1-(2-chloroacetyl)-3-(1-methylethyl)- -1H-2,1,3-benzothiadiazin-4 (3H)-one-2,2-dioxide, m.p. 133°-135° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04208514 |
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| Quelldatensatz | uspto-grants-1980_06 |
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| ORD ID | ord-fc14f0eb9e5741ebac892d99d9681697 |
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| Quellennotiz | uspto-grants-1980_06 |
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