HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787730Generated: October 30, 2026
Hydrochloric Acid → 2-Chloro-4-hydroxybenzaldehyde
https://huagongshe.com/reaction/1787730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Chloro-4-hydroxybenzonitrile | HCID 592797 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-4-hydroxybenzaldehyde | HCID 185363 | 84% |
Reaction Steps
Diisobutylaluminium hydride (1M in hexane, 240 mL, 240 mmol) was added to a solution of 2-chloro-4-hydroxybenzonitrile (15 g, 97.7 mmol) in tetrahydrofuran (200 mL), cooled to −78° C., and the mixture was stirred at this temperature for 1 hour then at room temperature for 18 hours. The mixture was then cooled to 0° C. and 1M hydrochloric acid (80 mL) was added dropwise. The reaction mixture was diluted with water (200 mL) and filtered, washing through with ethyl acetate (×2). The layers of the filtrate were separated and the organic solution was dried over magnesium sulfate and concentrated in vacuo. Trituration of the residue with dichloromethane afforded the title compound as a solid in 84% yield, 12.92 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511057B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-00ea2eff8b1942c3a6542fb6da338ae6 |
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| Source note | uspto-grants-2009_03 |
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