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HRID 324237作成日:2026年10月25日

4,4-Dimethyl-7-nitro-3,4-dihydronaphthalen-1(2H)-one → 7-Amino-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one

https://huagongshe.com/reaction/324237

反応式

関与物質

役割名称HCID仕込み量
反応物4,4-Dimethyl-7-nitro-3,4-dihydronaphthalen-1(2H)-oneHCID 13463292—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物7-Amino-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-oneHCID 15462841—

反応手順

A solution of 230.0 mg (1.05 mmol) 3,4-dihydro-4,4-dimethyl-7-nitro-1(2H)-naphthalenone (Compound Y) in 5.0 ml of EtOAc was stirred at room temperature with a catalytic amount of 10% Pd-C under 1 atm of H2 for 24 hours. The catalyst was removed by filtration through a pad of Celite, and the filtrate concentrated under reduced pressure to give the title compound as a dark green oil. 1H NMR (CDCl3): δ 7.30 (1H, d, J=2.7 Hz), 7.22 (1H, d, J=8.4 Hz), 6.88 (1H, dd, J=2.7, 8.5 Hz), 2.70 (2H, t, J=6.6 Hz), 1.97 (2H, t, J=6.6 HZ), 1.34 (6H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06218128B1
出典データセットuspto-grants-2001_04
ORD IDord-5ab6b8f98c95464e8510325b7b6ce587
出典メモuspto-grants-2001_04