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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1054Erstellt: 24. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → Methyl 6-methoxybenzofuran-2-carboxylate

https://huagongshe.com/de/reaction/1054

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktMethyl 2-formyl-5-methoxyphenoxyacetateHCID 19364036—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 6-methoxybenzofuran-2-carboxylateHCID 301696457%

Reaktionsschritte

A mixture of methyl 2-formyl-5-methoxyphenoxyacetate (27.7 g), 1,8-diazabicyclo[5.4.0]-7-undecene (40.8 g) and toluene (200 ml) was heated under refluxing conditions for 4 hours. The reaction mixture was concentrated under reduced pressure; after 6N hydrochloric acid was added, the residue was extracted with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; 10% hydrochloric acid-methanol (30 ml) was added to the residue, followed by heating at 70° to 80° C. for 4 hours. The reaction mixture was concentrated under reduced pressure; water was added, followed by extraction with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; the residue was subjected to silica gel column chromatography. From the fraction eluted with chloroform-hexane (1:2, v/v), methyl 6-methoxybenzofuran-2-carboxylate (14.3 g, 57%) was obtained, which was then recrystallized from dichloromethane-isopropyl ether to yield colorless prisms having a melting point of 97° to 98° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723479
Quelldatensatzuspto-grants-1998_03
ORD IDord-4b3d1be49f204b63a88b6e40011ab757
Quellennotizuspto-grants-1998_03