HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30890Erstellt: 24. Oktober 2026
Sulfuryl chloride → 2-Chloro-5-(trifluoromethyl)-1,3-benzothiazole
https://huagongshe.com/de/reaction/30890
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sulfuryl chloride | HCID 24648 | — |
| Edukt | 5-(trifluoromethyl)-1,3-benzothiazole-2-thiol | HCID 178419087 | — |
| Produkt | 2-Chloro-5-(trifluoromethyl)-1,3-benzothiazole | HCID 21985849 | 94% |
Reaktionsschritte
Sulfuryl chloride (9.09 g, 67.33 mmol) was added with stirring to 2-mercapto-5-(trifluoromethyl)benzothiazole (2.64 g, 11.22 mmol) over a period of 5 minutes. The reaction mixture was then allowed to stand for approximately 1 h. Ice water was added to the reaction mixture with stirring to decompose the excess of sulfuryl chloride, and the product was then extracted with ethyl acetate. The organic layer was washed with water (3×) and brine, dried over anhydrous Na2SO4 and concentrated. The resulting solid was dissolved in EtOAc and filtered though a short silica-gel column, eluting with EtOAc, to give 2-chloro-5-(trifluoromethyl)benzothiazole (2.50 g, 94%). LC-MS m/z 238.0 (MH+), ret. time 2.55 min; 1H NMR (400 MHz, DMSO-d6) δ 7.81 (d, 1H), 8.38 (m, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07423156B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-921fd12bd97a499788225f411c64e142 |
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| Quellennotiz | uspto-grants-2008_09 |
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