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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016564Generated: November 2, 2026

Acetic Acid → N-(2-isopropoxybenzyl)-2-phenoxyaniline

https://huagongshe.com/reaction/1016564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzenamine, 2-phenoxy-HCID 75899—
Reactant2-(Propan-2-yloxy)benzaldehydeHCID 250078—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductN-(2-isopropoxybenzyl)-2-phenoxyanilineHCID 1840721379.6%

Reaction Steps

To a solution of 1.64 g of 2-isopropoxybenzaldehyde in 10 ml of methanol was added 1.85 g of 2-aminodiphenyl ether, and then the mixture was stirred at room temperature for 30 minutes and cooled on ice-water. To the cooled reaction solution was gradually added 1.50 g of sodium borohydride, followed by stirring under ice-cooling for 30 minutes and then at room temperature for 30 minutes. An aqueous acetic acid solution (1.5 ml of acetic acid—30 ml of water) was added dropwise to the reaction solution, followed by stirring at room temperature for 10 minutes. After extraction 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 filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate−hexane=1:25) to give 2.65 g of N-(2-isopropoxybenzyl)-2-phenoxyaniline as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476056B2
Source datasetuspto-grants-2002_11
ORD IDord-29ab0b1bd26945fc803b70a83fa4f4aa
Source noteuspto-grants-2002_11