Nitric Acid → 2,3-Dihydro-1'-acetyl-5-nitrospiro[benzofuran-2,4'-piperidine]
反応式
[N+:1]([O-:4])(O)=[O:2].[C:5]([N:8]1[CH2:13][CH2:12][C:11]2([CH2:17][C:16]3[CH:18]=[CH:19][CH:20]=[CH:21][C:15]=3[O:14]2)[CH2:10][CH2:9]1)(=[O:7])[CH3:6].O>C(O)(=O)C>[C:5]([N:8]1[CH2:13][CH2:12][C:11]2([CH2:17][C:16]3[CH:18]=[C:19]([N+:1]([O-:4])=[O:2])[CH:20]=[CH:21][C:15]=3[O:14]2)[CH2:10][CH2:9]1)(=[O:7])[CH3:6]参加物
反応条件
- 温度
- 100 °C
実験手順
3.8 g of nitric acid (sp gr 1.42) in 30 ml of glacial acetic acid is added dropwise to a stirred solution of 4.7 g of 2,3-dihydro-1'-acetylspiro[benzofuran-2,4'-piperidine] in 65 ml of glacial acetic acid. After total addition, the reaction mixture is slowly heated to 100° C. over a 2 hour span and then cooled and poured into 500 ml of water. The diluted mixture is extracted with chloroform and the chloroform extracts are washed sequentially with a saturated sodium bicarbonate solution, a saturated sodium chloride solution and then dried. The chloroform is removed under reduced pressure. The residue is triturated with ether causing an orange precipitate, which is collected and recrystallized first from an ethyl alcohol-ether mixture and then from ethyl alcohol to provide the product, 2,3-dihydro-1'-acetyl-5-nitrospiro[benzofuran-2,4'-piperidine], mp 149°-150° C.
後処理
- additionAfter total addition
- temperaturecooled
- extractionThe diluted mixture is extracted with chloroform
- washthe chloroform extracts are washed sequentially with a saturated sodium bicarbonate solution
- dry with materiala saturated sodium chloride solution and then dried
- customThe chloroform is removed under reduced pressure
- customThe residue is triturated with ether causing an orange precipitate, which
- customis collected
- customrecrystallized first from an ethyl alcohol-ether mixture
出典と根拠
- ORDレコード
- ord-962b27478bb0484a82381b574ac38ac4
- 出典データセット
- uspto-grants-1979_08
- 特許番号
- US04166120
反応ノート
読み込み中…