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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41444Erstellt: 24. Oktober 2026

Tetrahydrofuran → 5-Isopropenyl-2,4-dimethoxy-benzoic acid methyl ester

https://huagongshe.com/de/reaction/41444

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktCesium carbonateHCID 10796—
EduktMethyl 5-bromo-2,4-dimethoxybenzoateHCID 3859236—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-Isopropenyl-2,4-dimethoxy-benzoic acid methyl esterHCID 59263148—

Reaktionsschritte

To potassium isopropylidene trifluoroborate (4.87 g, 32.7 mmol) and 5-bromo-2,4-dimethoxybenzoic acid methyl ester (7.5 g, 27.3 mmol) in THF (195 ml) was added Cs2CO3 (26.6 g, 81.8 mmol) in water (39 ml). The reaction was degassed and Pd(PPh3)4 (1.58 g, 1.36 mmol) added. The reaction was heated at reflux for three days then quenched by adding water and extracted with EtOAc (×2). The combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated to leave an orange solid. The product was taken up in EtOAc again and the precipitate filtered. The filtrate was evaporated to dryness to yield 5-isopropenyl-2,4-dimethoxy-benzoic acid methyl ester (6.2 g). 1H NMR (Me-d3-OD) 7.68 (1H, s), 6.66 (1H, s), 5.10-5.08 (1H, m), 5.02-5.00 (1H, m), 3.93 (3H, s), 3.92 (3H, s), 3.84 (3H, s), 2.08-2.06 (3H, m). MS: [M+H]+ 237.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530469B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ffbebf3f17d54c9a9a80f76eb51f7824
Quellennotizuspto-grants-2013_09