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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2165080Erstellt: 25. Oktober 2026

Ethyl Acetate → HCID 12564414, Verbindung

https://huagongshe.com/reaction/2165080

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktMethanesulfonyl chlorideHCID 31297—
EduktEthyl 5-chlorobenzofuran-2-carboxylateHCID 2799299—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 12564414HCID 1256441453,2%

Reaktionsschritte

To a suspension of ethyl-5-chloro-benzofuran carboxylate (1.05 g), prepared according to Helv. Chim. Acta., 818 (1935), in tetrahydrofuran (10 ml) was added lithium aluminum hydride (0.1 g). The mixture was stirred at room temperature for 1 hour. Ethyl acetate (50 ml) was slowly added to the reaction mixture, and the whole mixture was poured onto water (50 ml). The organic extract was separated, washed with water (2×25 ml), dried and evaporated to obtain 2-hydroxymethyl-5-cnlorobenzofuran as an oil [0.87 g; 'HNMR (CDCl3, 60 MHz): 4.6 (s, 2H), 6.6-7.4 (m, 4H)]. This material was added to a solution of methanesulfonyl chloride (1.15 g) in methylene chloride (20 ml) containing pyridine (1 ml). After stirring the reaction overnight it was poured onto ice-water (20 ml) and the organic extract was first washed with 10% HCl (5 ml) and then with water (2×10 ml). The washed extract was dried and evaporated to obtain 2-chloromethyl-5-chlorobenzofuran as a clear oil (yield: 0.5 g); HNMR (CDCl3, 60 MHz): 4.65 (s, 2H), 6.6 (s, 1H), 6.8-7.4 (m, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04939140
Quelldatensatzuspto-grants-1990_07
ORD IDord-74ec5ea09a564d7285053e9812c612c1
Quellennotizuspto-grants-1990_07