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4,4-Dimethyl-7-nitro-3,4-dihydronaphthalen-1(2H)-one → 7-Amino-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one
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)-one | HCID 13463292 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 7-Amino-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06218128B1 |
| 出典データセット | uspto-grants-2001_04 |
| ORD ID | ord-5ab6b8f98c95464e8510325b7b6ce587 |
| 出典メモ | uspto-grants-2001_04 |