HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824702Generated: October 31, 2026
Hydrochloric Acid → 5-Tert-butyl-2-methoxybenzoyl chloride
https://huagongshe.com/reaction/1824702
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 5-(tert-butyl)-2-methoxybenzoate | HCID 15724682 | — |
| Reactant | Sodium hydroxide--water (1/1/1) | HCID 23719242 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Tert-butyl-2-methoxybenzoyl chloride | HCID 22143100 | — |
Reaction Steps
To a solution of 3.8 g of 5-(tert-butyl)-2-methoxybenzoic acid methyl ester in MeOH (30 mL) was added 50% NaOH-water solution (1 mL). The resulting solution was stirred at room temperature for 3 hr. After the reaction was complete, the pH was adjusted to pH=2–3 using 1M HCl. The reaction mixture was collected by extraction with ethylacetate and water three times. The organic layer was dried over anhydrous magnesium sulfate (MgSO4) and evaporated under reduced pressure. After recrystallization, the final product yielded 3.4 g (96%). Without further purification a solution of 3.4 g of 5-(tert-butyl)-2-methoxybenzoic acid in 20 mL CH2Cl2 was slowly treated with SOCl2 (1.2 eq). The resulting solution was stirred at room temperature for 2 hr. The reaction mixture was evaporated under reduced pressure and dried in a vacuum oven overnight to yield 3.4 g (91.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045520B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-e8cd4a3a2227436c8f83a80cbdc0adba |
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| Source note | uspto-grants-2006_05 |
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