HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625773Generated: November 2, 2026
Hydrochloric Acid → 5-Bromo-2-methylbenzaldehyde
https://huagongshe.com/reaction/1625773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 5-bromo-N-methoxy-N,2-dimethylbenzamide | HCID 65307193 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-2-methylbenzaldehyde | HCID 10420289 | 92.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785403B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-679f9ea7cdb14178a6642f459d0543b5 |
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| Source note | uspto-grants-2014_07 |
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