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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847591Generated: October 25, 2026

1,5-Diphenylpentan-3-one → N-(1,5-Diphenylpent-3-yl)hydroxylamine

https://huagongshe.com/reaction/847591

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-Diphenylpentan-3-oneHCID 21496—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventIsopropanolHCID 3776—
ProductN-(1,5-Diphenylpent-3-yl)hydroxylamineHCID 2291003530.6%

Reaction Steps

A solution of 0.37 g (1.55 mmol) of 1,5-diphenyl-3-pentanone in 20 ml of 2-propanol was treated with 0.22g (3.1 mmol) of hydroxylamine hydrochloride and 0.31 g (4.7 mmol) of anhydrous sodium acetate. After being stirred for 10 min, the mixture was treated with 0.20 g (3.2 mmol) of sodium cyanoborohydride and stirred at ambient temperature for 16 h. After concentration in vacuo, the residue was taken up in ethyl acetate, washed sequentially with aqueous NaHCO3 and saturated brine, dried over MgSO4, and concentrated. Flash chromatography using 40% ethyl acetate in chloroform gave 121 mg (31%) of the desired compound (Rf 0.16, 30% ethyl acetate in chloroform) as a white solid, m.p. 54°-55° C. 1H NMR (CDCl3) δ 1.7-1.85 (m, 2H), 1.85-2.0 (m, 2H), 2.6-2.75 (m, 4H), 2.90 (pentet, J=6 Hz, 1H), 5.22 (br, 2H), 7.1-7.35 (m, 10H). Mass spectrum (M+H)+ =256.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05142056
Source datasetuspto-grants-1992_08
ORD IDord-44de30a433df468a9d7567e2a42897de
Source noteuspto-grants-1992_08