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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454456Generated: October 31, 2026

Pyridine → 2-(Acetyloxy)-5-tert-butylbenzoic acid

https://huagongshe.com/reaction/454456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-(1,1-Dimethylethyl)salicylic acidHCID 85281—
SolventDichloromethaneHCID 6344—
Product2-(Acetyloxy)-5-tert-butylbenzoic acidHCID 12274488—

Reaction Steps

Pyridine (0.034 mL) and acetic anhydride (0.034 mL) were sequentially added to a methylene chloride (0.54 mL) solution of 5-tert-butylsalicylic acid (0.054 g), followed by stirring at room temperature for 2 hours. The solvent was evaporated under reduced pressure, and 1 mol/L hydrochloric acid and ethyl acetate were added to the residue. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 100-90% chloroform/methanol] to obtain 0.049 g of 2-acetoxy-5-tert-butylbenzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-393bfbc670f34754be83d7d354a19086
Source noteuspto-grants-2013_07