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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 509177Erstellt: 26. Oktober 2026

4-Bromobenzaldehyde → p-Bromobenzhydryl alcohol

https://huagongshe.com/reaction/509177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromobenzaldehydeHCID 70741—
EduktHCID 178418255HCID 178418255—
LösungsmittelTetrahydrofuranHCID 8028—
Produktp-Bromobenzhydryl alcoholHCID 9822165,1%

Reaktionsschritte

To a solution of p-bromobenzaldehyde 10 (4 g, 21.6 mmol) in THF (20 mL) was added phenyl magnesium bromide (22.7 mL, 22.7 mmol) and the reaction mixture was stirred at room temperature for 30 minutes, quenched with water and partially concentrated under vacuum. The crude material was dissolved in ethyl acetate and washed with water. The organic layer was separated, dried over Na2SO4, filtered and concentrated. The residue was purified via prep-HPLC (ISCO) in silica gel column with a gradient of ethyl acetate (5-45%) in hexanes to afford title compound 11 as a colorless oil (3.7 g, 65%). 1H NMR (DMSO-d6) δ (ppm): 7.49-7.45 (m, 2H), 7.36-7.17 (m, 7H), 5.98 (d, J=4.1 Hz, 1H), 5.68 (d, J=3.9 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096565B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-7bfae734ebab4c12836f611a56949d96
Quellennotizuspto-grants-2015_08