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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859539Generated: October 29, 2026

Hydrochloric Acid → 5-tert-Butyl-4-hydroxy-2-methylbenzaldehyde

https://huagongshe.com/reaction/1859539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant6-tert-Butyl-m-cresolHCID 6937—
ReactantEthyl orthoformateHCID 31214—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventChlorobenzeneHCID 7964—
Product5-tert-Butyl-4-hydroxy-2-methylbenzaldehydeHCID 11286988—

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528510B1
Source datasetuspto-grants-2003_03
ORD IDord-04c1366301e14829bd9dca0f06492674
Source noteuspto-grants-2003_03