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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655207Erstellt: 24. Oktober 2026

Sodium hydride → trans 2-Quinolin-6-yl-cyclopropanecarboxylic acid ethyl ester

https://huagongshe.com/de/reaction/655207

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktTrimethyloxosulphonium chlorideHCID 197819—
EduktHCID 68531514HCID 68531514—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkttrans 2-Quinolin-6-yl-cyclopropanecarboxylic acid ethyl esterHCID 8664154059,3%

Reaktionsschritte

To a suspension of sodium hydride (71 mg, 1.76 mmol) in DMSO (3 mL) under nitrogen atmosphere was added trimethylsulfoxonium chloride (261 mg, 2.03 mmol). After stirring at room temperature for 30 minutes, a solution of 3-quinolin-6-yl-acrylic acid ethyl ester (200 mg, 0.881 mmol) in DMSO (2 mL) was added dropwise. The reaction mixture was stirred at room temperature for 2.5 h and quenched with a saturated aqueous solution of ammonium chloride. The mixture was extracted with ethyl acetate (2×) and the combined organic layers were washed with brine (3×) and adsorbed on silica gel. Purification on silica gel with 0-80% gradient of ethyl acetate in hexane provided 126 mg of product as a white solid. NMR 500 MHz (DMSO) δ 1.22 (t, 3H), 1.55 (m, 2H), 2.10 (m, 1H), 2.64 (m, 1H), 4.13 (q, 2H), 7.50 (dd, 1H), 7.58 (dd, 1H), 7.80 (d, 1H), 7.93 (d, 1H), 8.26 (dd, 1H), 8.84 (dd, 1H); MS (m/z) 242 [M+H+]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071581B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-9dc7e8a11d014e5e835963c5cedf1807
Quellennotizuspto-grants-2011_12