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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016580Generated: October 30, 2026

Acetic Acid → N-acetyl-N-(2-acetyloxybenzyl)-2-phenoxyaniline

https://huagongshe.com/reaction/1016580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzenamine, 2-phenoxy-HCID 75899—
Reactant2-Formylphenyl acetateHCID 237228—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductN-acetyl-N-(2-acetyloxybenzyl)-2-phenoxyanilineHCID 9820979—

Reaction Steps

In 30 ml of methanol were dissolved 1.74 g of 2-acetoxybenzaldehyde and 1.85 g of 2-phenoxyaniline, and after stirring at room temperature for an hour, 3.00 g of sodium borohydride was added, followed by stirring at the same temperature for 30 minutes. To the reaction solution was added dropwise an aqueous acetic acid solution (3.0 ml of acetic acid and 60 ml of water), and after stirring at room temperature for 10 minutes, the mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the solvent was concentrated under reduced pressure. A solution of the residue and 4 ml of triethylamine in 50 ml of methylene chloride was cooled to 0° C., and 2.00 ml of acetyl chloride was added dropwise with stirring, followed by stirring at room temperature for 20 minutes. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with 0.5 N hydrochloric acid, a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, successively, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the solvent was concentrated under reduced pressure to give a crude N-acetyl-N-(2-acetyloxybenzyl)-2-phenoxyaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476056B2
Source datasetuspto-grants-2002_11
ORD IDord-b2f0443a2b4d4ffd904a3bb8881f4281
Source noteuspto-grants-2002_11