Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726389Generated: November 3, 2026

Pyridine → HCID 18446923, compound

https://huagongshe.com/reaction/1726389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-Bromo-1-indanoneHCID 520695—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventEthanolHCID 702—
ProductHCID 18446923HCID 1844692398.3%

Reaction Steps

To 5-bromoindanone (6.03 g) in 40 mL ethanol was added 3.58 g methoxylamine hydrochloride and 3.5 mL pyridine. The mixture was stirred at ambient temperature for 1 hour and heated at 80° C. for 3 hours. The volatiles were removed under vacuum and the solid residue partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The ethyl acetate was washed with brine, dried over magnesium sulfate, filtered, and evaporated under vacuum to yield 6.74 g (98% yield) of a tan solid. 1H NMR (CDCl3) was consistent with an isomeric mixture of the desired structure, with the E oxime isomer as the major component. LC/MS indicated 2 close peaks, both with a M+1 molecular ion of m/z 242.0 by positive ESI.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491829B2
Source datasetuspto-grants-2009_02
ORD IDord-6154153a703f4fd0ba7551b858792695
Source noteuspto-grants-2009_02