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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68132Generated: October 30, 2026

Pyridine → HCID 76802937, compound

https://huagongshe.com/reaction/68132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 67417069HCID 67417069—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 76802937HCID 7680293794%

Reaction Steps

1-(3-Propoxy-5,6,7,8-tetrahydronaphthalen-2-yl)ethanone (8.88 g, 38.2 mmol) was dissolved in a mixed solvent of chloroform (20 ml) and methanol (80 ml). Hydroxylamine hydrochloride (4.05 g, 58.2 mmol) and pyridine (9.46 ml, 117 mmol) were added to the solution and stirred for 16 hours while heating under reflux. The reaction mixture was cooled to room temperature, and then concentrated to dryness under reduced pressure. 2N hydrochloric acid (30 ml) and water were added to the residue, followed by extraction using dichloromethane. The thus-obtained organic layer was concentrated to dryness under reduced pressure, and the residue was then purified using silica gel column chromatography (n-hexane: ethyl acetate=5:1). The purified product was concentrated to dryness under reduced pressure, giving a pale yellow powder of 1-(3-propoxy-5,6,7,8-tetrahydronaphthalen-2-yl)ethanone oxime (8.87 g, yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045108E1
Source datasetuspto-grants-2014_09
ORD IDord-8bd7e5421fc2466a983608bb645ea4df
Source noteuspto-grants-2014_09