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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1055Erstellt: 23. Oktober 2026

Ethyl Acetate → Methyl 6-hydroxy-1-benzofuran-2-carboxylate

https://huagongshe.com/de/reaction/1055

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktBoron tribromideHCID 25134—
EduktMethyl 6-methoxybenzofuran-2-carboxylateHCID 3016964—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 6-hydroxy-1-benzofuran-2-carboxylateHCID 1208297273%

Reaktionsschritte

Boron tribromide (24.9 g) was added dropwise to a solution of methyl 6-methoxybenzofuran-2-carboxylate (18.6 g) in dichloromethane (200 ml) at 0° C., followed by stirring at room temperature for 1 day. The reaction mixture was poured over ice water; ethyl acetate (300 ml) was added. After the organic layer was washed with water and dried (MgSO4), the solvent was distilled off; 10% hydrochloric acid-methanol (60 ml) was added to the residue, followed by heating at 70° to 80° C. for 5 hours. The reaction mixture was concentrated under reduced pressure; the resulting crystals of methyl 6-hydroxybenzofuran-2-carboxylate (10.75 g) were collected by filtration using diethyl ether-isopropyl ether (2:1, v/v). The filtrate was concentrated; the residue was subjected to silica gel column chromatography. From the fraction eluted with diethyl ether-hexane (1:2, v/v), methyl 6-hydroxybenzofuran-2-carboxylate (1.75 g) was obtained (total yield 73%), which was then recrystallized from diethyl ether-isopropyl ether to yield colorless prisms having a melting point of 176° to 177° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723479
Quelldatensatzuspto-grants-1998_03
ORD IDord-c5d94e5973074b06af209206e6641b73
Quellennotizuspto-grants-1998_03