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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593722Erstellt: 24. Oktober 2026

3-Bromo-2-fluorobenzaldehyde → (3-Bromo-2-fluorophenyl)(4-fluorophenyl)methanol

https://huagongshe.com/de/reaction/593722

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Bromo-2-fluorobenzaldehydeHCID 22019361—
EduktHCID 178418676HCID 178418676—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(3-Bromo-2-fluorophenyl)(4-fluorophenyl)methanolHCID 86730390—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 3-bromo-2-fluorobenzaldehyde (0.150 g, 0.739 mmol) in THF (3.21 mL) cooled to −78° C. was added (4-fluorophenyl)magnesium bromide (0.443 mL, 0.887 mmol). The reaction mixture was maintained at −78° C. for at least 1 hr, then allowed to warm to room temperature slowly over 2 hr. The reaction was quenched with a saturated aqueous solution of NH4Cl. The reaction mixture was diluted with CH2Cl2 and the layers were separated. The aqueous phase was extracted with CH2Cl2 (2×). Organics were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a yellow residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242967B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-c9632efbb6ef4d2c994b06af3aa332dc
Quellennotizuspto-grants-2016_01