HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716806Generated: November 3, 2026
Hydrochloric Acid → 2-Bromo-4-hydroxybenzaldehyde
https://huagongshe.com/reaction/716806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Bromo-4-hydroxybenzonitrile | HCID 13042251 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Bromo-4-hydroxybenzaldehyde | HCID 11084866 | — |
Reaction Steps
To a solution of 2-bromo-4-hydroxy-benzonitrile (Intermediate 7, 2000 mg, 10.1 mmol) in DCM (50 mL) and THF (10 mL), at 0° C., diisobutylaluminum hydride 1M in toluene (20.2 ml, 20.2 mmol) was slowly added (10 min) and the reaction mixture was stirred at the same temperature for 1 hour. Then 40 ml of HCl 2M were added and the reaction mixture was warmed at 40° C. for 30 minutes. After cooling ethyl acetate (100 ml) was added and two phases were separated. The organic layer was washed with brine (3×100 ml) dried over sodium sulphate and concentrated under vacuum to give the title compound (1950 mg) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193704B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-6bd3287dc33b418e83203ceef8eb8dac |
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| Source note | uspto-grants-2015_11 |
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