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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303530Generated: October 26, 2026

Benzaldehyde, 2-ethoxy- → alpha-(2-Ethoxyphenyl)-N-tert-butylnitrone

https://huagongshe.com/reaction/2303530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehyde, 2-ethoxy-HCID 11950—
ReactantN-tert-butylhydroxylamineHCID 98586—
SolventChloroformHCID 6212—
Productalpha-(2-Ethoxyphenyl)-N-tert-butylnitroneHCID 8505454578%

Reaction Steps

2-Ethoxybenzaldehyde (12.0 g, 79.90 mmol) and N-tert-butylhydroxylamine (10.69 g, 119.86 mmol) were mixed in chloroform with molecular sieves (50 g, 4 A) and silica gel (10 g). The mixture was sealed under argon gas and stirred for 70 h at room temperature. The mixture was then filtered and the solid washed with ethyl acetate and the combined solution was rotary evaporated. Pentane (50 mL) was added to the liquid residue and isolation of the resulting solid afforded 13.79 g (78.0% yield) of the title compound as white crystals, m.p. 58.3° C. (Rf=0.55 on a silica gel plate using ethyl acetate as the eluant).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433008B1
Source datasetuspto-grants-2002_08
ORD IDord-44a6e80480294fad800568d317e2a17b
Source noteuspto-grants-2002_08