HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178763Generated: October 30, 2026
Hydrochloric Acid → 2-Bromo-5-(trifluoromethyl)benzaldehyde
https://huagongshe.com/reaction/2178763
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Bromo-5-(trifluoromethyl)benzonitrile | HCID 12223980 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Bromo-5-(trifluoromethyl)benzaldehyde | HCID 7018047 | — |
Reaction Steps
To a solution of 2-bromo-5-(trifluoromethyl)benzonitrile (10.0 g, 40 mmol) in dichloromethane (100 mL) was dropwise added a 1.0 M solution of diisobutylaluminum hydride in hexane (48 mL). The resulting solution was stirred under nitrogen at ambient temperature for 1 h and was then diluted by addition of ether (100 mL). After cooling in an ice bath, a 3 N solution of HCl was carefully added, and the mixture was vigorously stirred at ambient temperature for 15 min. The organic layer was washed with brine, dried (MgSO4) and evaporated. The resulting oil was purified by flash chromatography (5% EtOAc/hexane) affording 5 g of 2-bromo-5-trifluoromethylbenzaldehyde. 1H NMR (CDCl3) δ 10.39 (s, 1H), 8.18 (d, J=2 Hz, 1H), 7.82 (d, J=8.8 Hz, 1H), 7.70 (dd, J=8.5 Hz, 2 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067921B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-8be073957a644c1fb553c8d7efeaf595 |
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| Source note | uspto-grants-2015_06 |
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