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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303556Generated: October 27, 2026

Benzaldehyde, 4-(phenylmethoxy)- → alpha-(4Benzyloxyphenyl)-N-cyclopentylnitrone

https://huagongshe.com/reaction/2303556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehyde, 4-(phenylmethoxy)-HCID 78109—
ReactantN-cyclopentylhydroxylamineHCID 10219393—
SolventChloroformHCID 6212—
Productalpha-(4Benzyloxyphenyl)-N-cyclopentylnitroneHCID 7400825985.1%

Reaction Steps

A mixture of 4-benzyloxybenzaldehyde (20 g, 94.23 mmol), N-cyclopentylhydroxylamine (14.3 g, 141.34 mmol), molecular sieves (60 g, 4A) and silica gel (15 g) in chloroform (300 mL) was stirred at room temperature under argon atmosphere for 48 hrs and then was refluxed for an additional 3 hrs. The mixture was filtered and rotary evaporated to give crystals which were recrystallized from hexanes and EtOAc to provide the title compound as white crystals, 23.7 g, 85.1% yield), m.p. 115.1° C. (Rf=0.35 on a silica gel plate using hexanes:EtOAc, 1:1, v:v, as an eluant).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433008B1
Source datasetuspto-grants-2002_08
ORD IDord-0a67fed1351d478d8a740da89bd62d3e
Source noteuspto-grants-2002_08