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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725362Generated: November 2, 2026

1-Tetralone → N-(3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamine

https://huagongshe.com/reaction/1725362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-TetraloneHCID 10724—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventMethanolHCID 887—
ProductN-(3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamineHCID 7687663.9%

Reaction Conditions

Temperature22 °C

Reaction Steps

Add hydroxylamine hydrochloride (71.0 g, 1.03 mol) to a solution of α-tetralone (100.0 g, 0.68 mol) in 300 mL of methanol and stir the resulting solution at reflux for 2 hours. Cool the mixture to 20-24° C. and concentrate under reduced pressure. Dilute the residue with 1 L of water and extract with dichloromethane. Wash the organic layer with saturated aqueous sodium chloride, dry over sodium sulfate, filter, and concentrate under reduced pressure. Crystallize the residue from isopropanol to provide the desired compound as an off-white solid (70.0 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491716B2
Source datasetuspto-grants-2009_02
ORD IDord-7e05f2a32a9e4ca2b04a3ae1ffeae1c4
Source noteuspto-grants-2009_02