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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 656039Erstellt: 26. Oktober 2026

Triethylsilane → 5-bromo-3-(2,2-dimethyltetrahydro-thiopyran-4-yl)-1H-indole-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/656039

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylsilaneHCID 12052—
EduktTrimethylsilyl triflateHCID 65367—
Edukt2,2-Dimethyltetrahydro-4h-thiopyran-4-oneHCID 287564—
Eduktmethyl 5-bromo-1H-indole-7-carboxylateHCID 24728848—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-bromo-3-(2,2-dimethyltetrahydro-thiopyran-4-yl)-1H-indole-7-carboxylic acid methyl esterHCID 5933276452,1%

Reaktionsschritte

To a solution of 2,2-Dimethyl-tetrahydro-thiopyran-4-one (7.9 g, 55.1 mmol) in DCM (100 mL) was added TMSOTf (10 mL, 55.1 mmol) and 5-Bromo-1H-indole-7-carboxylic acid methyl ester (7.0 g, 27.6 mmol) at 0° C. After 2 hours, Et3SiH (15 mL, 110 mmol) was added at 0° C., then the mixture was stirred for 18 hours. The reaction mixture was quenched with sat. Sodium bicarbonate solution, extracted with DCM (3×100 mL). The combined organic layer was dried over MgSO4 and concentrated under vacuum. The residue was purified by column chromatography on silica gel (PE:EA=50:1 to 30:1) to give the title compound as a light yellow solid (5.5 g, 52%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071584B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-01dff079747a4e9b9b1242710ceafc5b
Quellennotizuspto-grants-2011_12