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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249919Erstellt: 25. Oktober 2026

Tetrahydrofuran → Methyl 2-amino-5-methoxy-3-methylbenzoate

https://huagongshe.com/reaction/249919

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktMethylboronic AcidHCID 139377—
EduktPotassium FluorideHCID 522689—
EduktTri-t-butylphosphoniumHCID 4060964—
EduktMethyl 2-amino-5-bromo-3-methoxybenzoateHCID 13894022—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
ProduktMethyl 2-amino-5-methoxy-3-methylbenzoateHCID 2028187373%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A mixture of methyl 2-amino-5-bromo-3-methoxybenzoate (6.50 g, 25 mmol), methylboronic acid (3.0 g, 50 mmol), potassium fluoride (5.8 g, 100 mmol) and tri-t-butylphosphonium tetrafluoroborte (0.87 g, 3.0 mmol) in THF (200 mL) was deoxygenated and then backfilled with argon. Tris(dibenzylideneacetone)dipalladium(0) (1.43 g, 1.5 mmol), was added and the mixture was heated at 70° C. for 17 h under an argon atmosphere. The reaction mixture was concentrated and the residue purified by column chromatography (silica gel, 0% to 5% EtOAc in hexanes) to afford methyl 2-amino-5-methoxy-3-methylbenzoate (3.55 g, 73%) 1H NMR consistent.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863271B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-35df134f9a174ac298eb7dd43559fd3c
Quellennotizuspto-grants-2011_01