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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848590Generated: November 3, 2026

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

https://huagongshe.com/reaction/1848590

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 numberUS08952161B2
Source datasetuspto-grants-2015_02
ORD IDord-f29a57735809484f81ea393a2aac5453
Source noteuspto-grants-2015_02