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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-hydroxybenzoic acidHCID 91821—
Reactant(S)-2-methyl-1-butanolHCID 2723602—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product(S)-2-methylbutyl 2-chloro-4-hydroxybenzoateHCID 1453355298.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04828754
Source datasetuspto-grants-1989_05
ORD IDord-e9e8abbd0ad04f1ea4ccc23168c3344d
Source noteuspto-grants-1989_05