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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482818Generated: October 30, 2026

Water → p-n-Tetradecyloxy-4-(2-methylbutoxycarbonyl)benzylideneaniline

https://huagongshe.com/reaction/482818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantp-(n-Tetradecyloxy)phenylamineHCID 191002—
Reactantp-(2-Methylbutoxycarbonyl)benzaldehydeHCID 13548338—
SolventTolueneHCID 1140—
Productp-n-Tetradecyloxy-4-(2-methylbutoxycarbonyl)benzylideneanilineHCID 13628479—

Reaction Steps

44.3 g of said p-(2-methylbutoxycarbonyl)benzaldehyde, 32 g of p-n-tetradecyloxyaniline, and 0.1 g of p-toluenesulfonic acid were dissolved in toluene. The solution was heated under reflux, and water generated in the dehydrating condensation was removed with a Dean-Stark condenser. After the reaction solution was cooled, the organic layer was washed with water, and the solvent (toluene) was distilled off in vacuum. The solid residue was recrystallized from ethanol to obtain yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576732
Source datasetuspto-grants-1986_03
ORD IDord-063c506506db4d19beb5dc80ac421b83
Source noteuspto-grants-1986_03