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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1501208Erstellt: 27. Oktober 2026

4-Bromo-3-fluorobenzaldehyde → 1-(4-Bromo-3-fluorophenyl)ethan-1-ol

https://huagongshe.com/reaction/1501208

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromo-3-fluorobenzaldehydeHCID 2783411—
EduktHCID 178418573HCID 178418573—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(4-Bromo-3-fluorophenyl)ethan-1-olHCID 71756542—

Reaktionsschritte

To a solution of 4-bromo-3-fluorobenzaldehyde (5 g, 24.75 mmol) in anhydrous tetrahydrofuran (100 mL) was added methyl magnesium bromide (3 M solution in tetrahydrofuran, 8.21 mL) at −45° C. under the atmosphere of nitrogen then stirred at room temperature. After 2 hours, LC-MS showed the desired product has received. The aqueous of ammonium chloride (15 mL) was added to quench the reaction, and extracted with ethyl acetate (50 mL), combined and concentrated the organic layers. The crude product was purified by column chromatography (petroleum ether/ethyl acetate=1:1) to give 1-(4-bromo-3-fluorophenyl)ethanol (4 g, 78%). LCMS (M+H+) m/z: calcd 217.97. found 218. 1H NMR (300 MHz, CD3OD): δ 7.92-7.87 (m, 1H), 7.23-7.19 (m, 1H), 7.07-7.10 (m, 1H), 4.80 (d, J=6.3 Hz, 1H), 1.41 (t, J=2.7 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09206128B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-86254549ae6742c5aa12c4c86923c28f
Quellennotizuspto-grants-2015_12