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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504668Generated: October 30, 2026

Hydrochloric Acid → 4-(Bromomethyl)-3-chlorobenzaldehyde

https://huagongshe.com/reaction/1504668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant4-(Bromomethyl)-3-chlorobenzonitrileHCID 13042093—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
Product4-(Bromomethyl)-3-chlorobenzaldehydeHCID 8667517780%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-(bromomethyl)-3-chlorobenzonitrile (4.8 g, 17 mmol) in toluene (50 mL) at 0° C. was added dropwise diisobutylaluminum hydride (DIBAL-H, 1.0 M solution in toluene; 23.9 mL), and the reaction mixture was stirred at 0° C. for 1 h. 10 M HCl in H2O (5 mL) was added until the reaction mixture turned to a white slurry and then additional 1 N HCl (20 mL) was added. The organic layer was collected and the aqueous layer was extracted with CHCl3. The combined organic layer was dried over Na2SO4 and concentrated under reduced pressure. The crude compound was purified by flash column chromatography (SiO2, 100-200 mesh; 5% EtOAc in n-Hexane) to afford the title compound as a white solid (3.8 g, 80%): mp 64-66° C.; 1H NMR (400 MHz, CDCl3) δ 10.00 (s, 1H), 7.92 (s, 1H), 7.78 (d, J=8.0 Hz, 1H), 7.64 (d, J=8.0 Hz, 1H), 4.60 (s, 2H); ESIMS m/z 232.78 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09215870B2
Source datasetuspto-grants-2015_12
ORD IDord-c5721851e29d466dba7a4b3116fabfbf
Source noteuspto-grants-2015_12