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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661630Generated: November 2, 2026

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

https://huagongshe.com/reaction/661630

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 numberUS08084614B2
Source datasetuspto-grants-2011_12
ORD IDord-1387bc7d6b674bc8aa50217c4c28cd7d
Source noteuspto-grants-2011_12