HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450293Erstellt: 23. Oktober 2026
Hexachloroethane → Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-4-chloro-1H-indol-5-yl ester
https://huagongshe.com/de/reaction/450293
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hexachloroethane | HCID 6214 | — |
| Edukt | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-1H-indol-5-yl ester | HCID 9975323 | — |
| Edukt | CID 53628100 | HCID 178418400 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-4-chloro-1H-indol-5-yl ester | HCID 9977109 | — |
Reaktionsschritte
Diethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-1H-indol-5-yl ester (9.26 g, 26.7 mmol) is dissolved in THF (250 mL), flushed with nitrogen and cooled to −78° C. TMEDA (5 mL, 33.1 mmol) is then added followed by sec-butyllithium (24.8 mL, 34.7 mmol) and the reaction is stirred for 30 minutes. Hexachloroethane (12.73 g, 53.8 mmol) in 50 mL of THF is added over 10 minutes to the reaction. The reaction is allowed to warm to room temperature overnight (15 hours). The reaction is cooled using an ice bath and a saturated ammonium chloride (aq) solution is added (150 mL). The mixture is then extracted with ethyl acetate, dried (sodium sulfate) and concentrated to obtain the title compound as an oil that is used without further purification. MS (ESI) m/z 381.1 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08486954B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-ed2e015faf7148bebe191541f8f80ee1 |
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| Quellennotiz | uspto-grants-2013_07 |
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