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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexachloroethaneHCID 6214—
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
EduktAmmonium ChlorideHCID 25517—
EduktDiethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-1H-indol-5-yl esterHCID 9975323—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDiethyl-carbamic acid 1-(tert-butyl-dimethyl-silanyl)-4-chloro-1H-indol-5-yl esterHCID 9977109—

Reaktionsbedingungen

Temperatur-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08486954B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-ed2e015faf7148bebe191541f8f80ee1
Quellennotizuspto-grants-2013_07