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HRID 1782655Erstellt: 24. Oktober 2026

Ethanol → [1,1'-Biphenyl]-4-carboxylicacid, 4'-bromo-, methyl ester

https://huagongshe.com/de/reaction/1782655

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
EduktMethyl 4-iodobenzoateHCID 69273—
Edukt(4-Bromophenyl)boronic acidHCID 79599—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkt[1,1'-Biphenyl]-4-carboxylicacid, 4'-bromo-, methyl esterHCID 737627—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of methyl 4-iodobenzoate, 9.38 g (35.8 mmol), 4-bromophenylboronic acid 7.18 g (35.8 mmol), Pd(PPh3)4, 2.07 g (1.79 mmol), in 180 mL of toluene and 100 mL of ethanol was heated to obtain a clear solution. To the solution was added 30 mL of 4.0M aq. Na2CO3. The reaction mixture refluxed for 4 h at 80° C. The mixture was cooled to room temperature and diluted with 300 mL ethyl acetate. The organic layer was washed with 2×300 mL portions of water, 2×300 mL portions of sat. aq. NaCl, and dried (MgSO4). After the solution was concentrated, the residue was purified by column chromatography (eluted with 7% EtOAc-Heptane) to afford the desired product in 7.8 g (78%) as a white solid. 1H NMR (CDCl3) 8.10 (d, 2H, J=9.0 Hz), 7.62 (d, 2H, J=9.0 Hz), 7.59 (d, 2H, J=9.3 Hz), 7.48 (d, 2H, J=9.3 Hz), 3.95 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07498356B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-f8b428ec23fd4237a150471823319346
Quellennotizuspto-grants-2009_03