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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625773Generated: November 2, 2026

Hydrochloric Acid → 5-Bromo-2-methylbenzaldehyde

https://huagongshe.com/reaction/1625773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant5-bromo-N-methoxy-N,2-dimethylbenzamideHCID 65307193—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-methylbenzaldehydeHCID 1042028992.8%

Reaction Steps

A solution of the above N-methoxy-N-methyl-5-bromo-2-methylbenzamide (12.2 g) in tetrahydrofuran (100 ml) was cooled to −78° C. under argon atmosphere. To the mixture was added dropwise diisobutyl aluminum hydride (1.0 M toluene solution, 75 ml), and the mixture was stirred at the same temperature for one hour. 10% aqueous hydrochloric acid solution (50 ml) was added thereto, and the mixture was warmed to room temperature. The mixture was extracted with ethyl acetate twice, and washed successively with a saturated aqueous sodium hydrogen carbonate solution and brine. The extract was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was solidified to give 5-bromo-2-methylbenzaldehyde (8.73 g). APCI-Mass m/Z 213/215 (M+H+MeOH−H2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-679f9ea7cdb14178a6642f459d0543b5
Source noteuspto-grants-2014_07