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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448878Generated: October 26, 2026

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

https://huagongshe.com/reaction/448878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-TetraloneHCID 10724—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventMethanolHCID 887—
ProductN-(3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamineHCID 76876108.7%

Reaction Steps

To a solution of α-tetralone (10 g, 68.5 mmol) in anhydrous MeOH (175 mL), hydroxylamine hydrochloride (7.6 g, 109.6 mmol) and triethylamine (15.3 mL, 109.6 mmol) were added. The mixture was stirred at room temperature for 16 hrs, followed by removal of the solvent in vacuo. The residue was dissolved in DCM, washed with water and brine, dried (Na2SO4), filtered and concentrated in vacuo to yield crude 3,4-dihydro-2H-naphthalen-1-one oxime (12 g). MS [M+H]+: 162.1; tR=2.03 min. (method 1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481738B2
Source datasetuspto-grants-2013_07
ORD IDord-e6abb06940f34a21842540b7f830e82c
Source noteuspto-grants-2013_07