Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241503Generated: October 30, 2026

Pyridine → 7-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oxime

https://huagongshe.com/reaction/241503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant7-Chloro-1,2,3,4-tetrahydronaphthalen-1-oneHCID 256677—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventMethanolHCID 887—
Product7-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oximeHCID 86699876100%

Reaction Conditions

Temperature24 °C

Reaction Steps

To a stirred solution of 7-chloro-1-tetralone CAS: 26673-32-5 (5.0 g; 27.68 mmol) in methanol (55 ml) was added pyridine (2.87 ml; 34.05 mmol) followed by a portion wise addition of methoxyamine hydrochloride (2.84 g; 34.05 mmol). The reaction mixture was stirred at 24° C. for 16 h under nitrogen. Methanol was removed under reduced pressure, the residue poured in water (300 ml) and 1N hydrochloric acid was added (100 ml). The solution was extracted with dichloromethane (3×150 ml). Combined organic layers were washed with water (300 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 6.22 g (100% of theory) of crude 7-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oxime as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653003B2
Source datasetuspto-grants-2014_02
ORD IDord-d23521188cca4cfaab81244a486e6095
Source noteuspto-grants-2014_02