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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593485Generated: October 30, 2026

Pyridine → 1H-Inden-1-one, 5-bromo-2,3-dihydro-, O-methyloxime

https://huagongshe.com/reaction/1593485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromo-1-indanoneHCID 520695—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventEthanolHCID 702—
Product1H-Inden-1-one, 5-bromo-2,3-dihydro-, O-methyloximeHCID 7301284097.5%

Reaction Steps

To a solution of 5-bromoindan-1-one (100 g, 0.47 mol) in ethanol (650 ml) under argon was added methoxylamine hydrochloride (198 g, 2.38 mol) and pyridine (125 ml). The mixture was heated under reflux for 2.5 hours, cooled to room temperature and poured into saturated aqueous sodium hydrogen carbonate solution. The mixture was extracted with ethyl acetate and the organic phase dried and concentrated in vacuo. The crude material was recrystallised from isopropanol to afford the title compound (110 g, 97%); 1H NMR (CDCl3) 7.52 (1H, d, J 8.3 Hz), 7.43 (1H, d, J 1 Hz), 7.35 (1H, dd, J 8.3, 1 Hz), 3.97 (3H, s), 2.99 (2H, m), 2.85 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297693B2
Source datasetuspto-grants-2007_11
ORD IDord-1909b37723f24a06af711ebb6d1cb86e
Source noteuspto-grants-2007_11