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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673529Generated: October 31, 2026

Aspirin → Tert-butyl 2-(2-acetoxybenzamido)-4-phenethylbenzoate

https://huagongshe.com/reaction/1673529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAspirinHCID 2244—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 2-amino-4-phenethylbenzoateHCID 58508624—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductTert-butyl 2-(2-acetoxybenzamido)-4-phenethylbenzoateHCID 67341697—

Reaction Steps

2.0 mL of methylene chloride, 2.7 μL of N,N-dimethylformamide and 0.061 mL of oxalyl chloride were added to 0.13 g of 2-acetoxybenzoic acid at room temperature sequentially and stirred at the same temperature for 1 hour. The reaction mixture was added to a mixed solution of 3.0 mL of methylene chloride and 0.45 mL of triethylamine containing 60 mg of tert-butyl 2-amino-4-phenethylbenzoate at room temperature and stirred at the same temperature for 1 hour. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, and the organic layer was separated, and the solvent was evaporated under reduced, pressure. The obtained residue was purified with silica gel column chromatography [Flash Tube 2008 manufactured by Trikonex Company, eluent; hexane; ethyl acetate=4:1] to obtain tert-butyl 2-(2-acetoxybenzamido)-4-phenethylbenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-93137a9debb2465c83562ce55122c5c8
Source noteuspto-grants-2011_08