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HRID 1078102作成日:2026年10月27日

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

https://huagongshe.com/reaction/1078102

反応式

関与物質

役割名称HCID仕込み量
反応物1,5-Diphenylpentan-3-oneHCID 21496—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物Sodium AcetateHCID 517045—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒IsopropanolHCID 3776—
生成物N-(1,5-Diphenylpent-3-yl)hydroxylamineHCID 2291003530.6%

反応手順

A solution of 0.37 g (1.55 mmol) of 1,5-diphenyl-3-pentanone in 20 ml of 2-propanol was treated with 0.22 g (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) δ1.7-1.85 (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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05545750
出典データセットuspto-grants-1996_08
ORD IDord-6cc1a4385b99425cb52c8c7e210cb436
出典メモuspto-grants-1996_08