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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2086937Erstellt: 25. Oktober 2026

Benzenesulfonyl chloride → 1-(Phenylsulfonyl)-1,5,6,7-tetrahydro-4H-indol-4-one

https://huagongshe.com/reaction/2086937

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
EduktSodium hydrideHCID 24758—
Edukt1,5,6,7-Tetrahydro-4H-indol-4-oneHCID 280229—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(Phenylsulfonyl)-1,5,6,7-tetrahydro-4H-indol-4-oneHCID 1343770985%

Reaktionsschritte

A stirred solution of 1,5,6,7-tetrahydro-4H-indol-4-one (5.0 g, 37.0 mmol) in THF is treated portionwise with NaH (60% dispersion in mineral oil, 1.5 g, 37.0 mmol) under N2 at room temperature, stirred for 0.5 hr, treated with benzene sulfonyl chloride (4.7 ml, 37.0 mmol), stirred for 24 hr, quenched with water and diluted with EtOAc. The phases are separated. The organic phase is washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, EtOAc/hexanes, 1/1 as eluent) to afford the title product as an off-white solid, 8.72 g (85% yield), mp 108-110° C., identified by NMR and mass spectral analyses.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06727270B2
Quelldatensatzuspto-grants-2004_04
ORD IDord-8094538fe8ee497da0857f8a1ee97d97
Quellennotizuspto-grants-2004_04