HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761823Generated: October 24, 2026
2-Chloro-4-hydroxybenzoic acid → (S)-2-methylbutyl 2-chloro-4-hydroxybenzoate
https://huagongshe.com/en/reaction/1761823
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-4-hydroxybenzoic acid | HCID 91821 | — |
| Reactant | (S)-2-methyl-1-butanol | HCID 2723602 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (S)-2-methylbutyl 2-chloro-4-hydroxybenzoate | HCID 14533552 | 98.1% |
Reaction Steps
2-Chloro-4-hydroxybenzoic acid (17.2 g: 100 mmols), 10.5 g (120 mmols) of (S)-2-methylbutanol and 0.17 g (1 mmol) of p-toluenesulfonic acid were refluxed in 100 ml of toluene on heating. Azeotropic water was removed with a Dean Stark trap. After water was no longer distilled off, the residue was left to cool up to room temperature. The resulting product was washed with a sodium bicarbonate aqueous solution until the aqueous phase became alkaline. The product was further washed with water and then with saturated sodium chloride aqueous solution, and dried with anhydrous sodium sulfate. Excess toluene and (S)-2-methylbutanol were mostly distilled off under reduced pressure and the residue was recrystallized from n-hexane to obtain 23.8 g of (S)-2-methylbutyl 2-chloro-4-hydroxybenzoate as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04828754 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-e9e8abbd0ad04f1ea4ccc23168c3344d |
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| Source note | uspto-grants-1989_05 |
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