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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305779Generated: October 25, 2026

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

https://huagongshe.com/reaction/2305779

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, 4A) 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 numberUS06441032B1
Source datasetuspto-grants-2002_08
ORD IDord-11b45f8ceea94f5cb8b60a5eb9327237
Source noteuspto-grants-2002_08