HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23466Generated: October 25, 2026
Hydrochloric Acid → 5-tert-Butyl-4-hydroxy-2-methylbenzaldehyde
https://huagongshe.com/reaction/23466
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 6-tert-Butyl-m-cresol | HCID 6937 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 5-tert-Butyl-4-hydroxy-2-methylbenzaldehyde | HCID 11286988 | — |
Reaction Steps
Aluminum chloride (26.6 g, 200 mmol) was added to chlorobenzene (40 mL), and the mixture was cooled to −10° C. A solution of 2-tert-butyl-5-methylphenol (16.4 g, 100 mmol) in triethyl orthoformate (32.5 g, 220 mmol) was added dropwise. When addition was complete, the reaction mixture was warmed to 0° C. to 5° C. and kept at that temperature for 6 hours. Five percent HCl (100 mL) was added, and the mixture was extracted with 1:1 EtOAC:toluene. The organic phase was extracted with 23% KOH (3×50 mL) and water (25 mL), and the water extract was combined with the KOH extracts. The pH of the combined aqueous extracts was adjusted to 4 with 37% HCl. The resulting precipitate was filtered, washed with water (3×50 mL), and dried to give the title compound, mp 171-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852711B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-d2ac3b7a52c4435a87fc980e037e3c53 |
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| Source note | uspto-grants-2005_02 |
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