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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1595457Erstellt: 27. Oktober 2026

Benzenesulfonyl chloride, 3,4-dichloro- → 1-(3,4-Dichloro-benzenesulfonyl)-1H-indole-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1595457

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
EduktSodium hydrideHCID 24758—
EduktMethyl 1H-indole-2-carboxylateHCID 70992—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(3,4-Dichloro-benzenesulfonyl)-1H-indole-2-carboxylic acid methyl esterHCID 2170508751%

Reaktionsschritte

Methyl indole-2-carboxylate (0.15 g) was dissolved in DMF and sodium hydride (41 mg) was added in a single portion. The reaction was stirred for 1 hour, then 3,4-dichlorobenzenesulphonyl chloride (0.25 g) was added in a single portion. Stirring was continued for a further 2 hours and then the reaction was quenched by the addition of water. The reaction mixture was partitioned between water and ethyl acetate. Combined organic extracts were dried (MgSO4) and concentrated in vacuo and the residue purified by column chromatography using isohexane-5% ethyl acetate as eluent to give the desired end product as a solid (51%). NMR δ (CDCl3) 3.96 (s, 3H), 7.22-8.20 (m, 8H); M/z (+) 384 (MH+), 352, 175.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06288103B1
Quelldatensatzuspto-grants-2001_09
ORD IDord-68781318143040b78dcc54e5d3867522
Quellennotizuspto-grants-2001_09