HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 900299Erstellt: 24. Oktober 2026
Tetrahydrofuran → (Tert-butyl)[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amine
https://huagongshe.com/de/reaction/900299
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Edukt | 5-Chlorothiophene-2-sulfonic acid tert-butylamide | HCID 10106323 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | (Tert-butyl)[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amine | HCID 22064462 | 108,2% |
Reaktionsschritte
A THF solution (1.5 mL) of 128 mg (0.50 mmol) of (tert-butyl)[(5-chloro(2-thienyl))sulfonyl]amine was cooled to −78° C. and treated with 954 μL (1.5 mmol) of a 1.6 M solution of butyl lithium in hexane. After 1 h, 159 mg (0.5 mmol) of bis(phenylsulfonyl)fluoroamine was added and the solution was allowed to warm to 23° C. The reaction was quenched with 1 mL of sat. NH4Cl, extracted 3 times with diethyl ether, dried (MgSO4), concentrated in vacuo to afford a quantitative yield (147 mg) of the desire product. 19F-NMR (CDCl3) δ (ppm): −113.4.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07358257B2 |
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| Quelldatensatz | uspto-grants-2008_04 |
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| ORD ID | ord-b9726075593e46f5a80025deb39017e5 |
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| Quellennotiz | uspto-grants-2008_04 |
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