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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910066Generated: October 31, 2026

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

https://huagongshe.com/reaction/910066

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 numberUS08022065B2
Source datasetuspto-grants-2011_09
ORD IDord-2886b1a562c343b59f883f558650f464
Source noteuspto-grants-2011_09