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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881793Generated: November 2, 2026

5-Methoxyindan-1-one → 5-Methoxyindan-1-one oxime

https://huagongshe.com/reaction/1881793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxyindan-1-oneHCID 78787—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Methoxyindan-1-one oximeHCID 288189—

Reaction Conditions

Temperature70 °C

Reaction Steps

5-Methoxy-2,3-dihydromden-1-one (Ig, 6.17 mmol) was added to a solution of hydroxylamine HCl (730 mg, 10.5 mmol) in 10 ml of water. The mixture was brought up to 70° C. and a solution of sodium acetate (1.4 g, 16.7 mmol) in 7 mL of H2O, 14 ml of MeOH, 3 ml of THF was added. After stirring for 1.5 h at 70° C., 10 ml of H2O was added to produce a precipitate and the suspension was allowed to stir for 2 h. The precipitate was collected by filtration to give 5-methoxy-2,3-dihydroinden-1-one oxime almost quantitatively and was used in the next step without further purification. The oxime (0.5 g, 2.82 mmol) was dissolved in MeOH and a catalytic amount of Raney nickel and 25 mL of ammonia solution in MeOH (7N) was added. The reaction was stirred at r.t. overnight under H2. The slurry was filtered over celite and concentrated in vacuo, diluted with EtOAc, washed with water and brine, dried over MgSO4, filtered, and concentrated in vacuo to give the crude title amine (yield, 45%). The crude amine was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318947B2
Source datasetuspto-grants-2012_11
ORD IDord-b5acdce661774062b0c643ae8e90ecdd
Source noteuspto-grants-2012_11