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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41927Generated: October 26, 2026

Acetophenone → (E)-N-[(4-nitrophenyl)methoxy]-1-phenylethanimine

https://huagongshe.com/reaction/41927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantHydroxylamine, O-((4-nitrophenyl)methyl)-, hydrochloride (1:1)HCID 74967—
Product(E)-N-[(4-nitrophenyl)methoxy]-1-phenylethanimineHCID 2510009277%

Reaction Steps

Acetophenone (20) (150 mg, 1.25 mmol) was condensed with compound 19 (280 mg, 1.37 mmol) according to the general procedure II-A defined above. After heating the reaction mixture for 2 h it was cooled and the solvent removed under reduced pressure. The resulting solid was filtered off and washed with cold isopropanol (3.0 mL) to afford the title compound CP30252 (258 mg, 77%) as a pale-yellow solid, m.p. 91.3-92.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536157B2
Source datasetuspto-grants-2013_09
ORD IDord-23a916c9fb6443c8ab25be0c5e823b60
Source noteuspto-grants-2013_09