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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003686Generated: October 31, 2026

3-Ethoxy-4-methoxybenzaldehyde → HCID 86587914, compound

https://huagongshe.com/reaction/1003686

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethoxy-4-methoxybenzaldehydeHCID 244728—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 21111947HCID 21111947—
SolventBenzeneHCID 241—
ProductHCID 86587914HCID 86587914—

Reaction Steps

3-Ethoxy-4-methoxybenzaldehyde (12.0 g, 0.0666 mol) and N-(4-methylpent-2-yl)hydroxylamine (9.36 g, 0.0799 mol) were mixed into benzene (200 mL) with p-toluenesulfonic acid monohydrate (1.0 g, 5.26 mol.). The mixture was refluxed for 16 hours under an argon atmosphere with a Dean-Stark trap to remove the generated water. The solution was rotary evaporated, dissolved in ethyl acetate, washed with 5 % aqueous sodium hydroxide solution, dried over magnesium sulfate, filtered and concentrated. The title compound was obtained as a white solid (17.07 g, 91.8% yield), m.p. 87.2° C. (Rf =0.31 on a silica gel plate using hexanes;EtOAc, 1:1, v/v, as an eluant). The N-(4-methyl-2-pentyl)hydroxylamine precursor was obtained by sodium cyanoborohydride reduction of 4-methyl-2-pentanone oxime in methanol, with hydrochloric acid catalysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046232
Source datasetuspto-grants-2000_04
ORD IDord-cc60d8a4634944fe9588d399096f08f9
Source noteuspto-grants-2000_04