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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509177Generated: October 27, 2026

4-Bromobenzaldehyde → p-Bromobenzhydryl alcohol

https://huagongshe.com/reaction/509177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzaldehydeHCID 70741—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Productp-Bromobenzhydryl alcoholHCID 9822165.1%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096565B2
Source datasetuspto-grants-2015_08
ORD IDord-7bfae734ebab4c12836f611a56949d96
Source noteuspto-grants-2015_08