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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546683Generated: October 31, 2026

Triethylamine → Benzyl (3,4,5-trifluorophenyl)acetate

https://huagongshe.com/reaction/546683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant3,4,5-Trifluorophenylacetic acidHCID 2777952—
ReactantSodium bicarbonate waterHCID 86585896—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductBenzyl (3,4,5-trifluorophenyl)acetateHCID 86628508—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (0.808 mL) and benzyl chloroformate (0.752 mL) were sequentially added dropwise to a solution of 3,4,5-trifluorophenylacetic acid (1 g) in methylene chloride (15 mL) at 0° C., and the reaction solution was stirred at 0° C. for five minutes. DMAP (64.4 mg) was added to the reaction solution which was then stirred at 0° C. for 30 minutes. Ethyl acetate and saturated sodium bicarbonate water were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system) to obtain 1.43 g of the title compound. The property values of the compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935815B2
Source datasetuspto-grants-2011_05
ORD IDord-0a109376805a4abd85f233325c4b350b
Source noteuspto-grants-2011_05