反応式
[CH2:1]([NH2:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[I:8][C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=1[C:11](Cl)=[O:12]>O1CCCC1>[CH2:1]([NH:7][C:11](=[O:12])[C:10]1[CH:14]=[CH:15][CH:16]=[CH:17][C:9]=1[I:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]参加物
4
実験手順
Solutions of 12.2 g hexylamine and 8.0 g o-iodobenzoyl chloride in a total of 20 ml tetrahydrofuran were reacted for 10 minutes. The tetrahydrofuran was removed by heating on a water bath at 65° for 10 minutes and 50 ml of water were added to precipitate the crude product. The precipitate was recovered as in Example 1 and recrystallized from a benzene/hexane mixture as white crystals, to yield 7.6 g of N-hexyl-o-iodobenzamide, m.p. 104°-105°, Rf 0.78.
後処理
- customThe tetrahydrofuran was removed
- temperatureby heating on a water bath at 65° for 10 minutes
- addition50 ml of water were added
- customto precipitate the crude product
- customThe precipitate was recovered as in Example 1
- customrecrystallized from a benzene/hexane mixture as white crystals
出典と根拠
- ORDレコード
- ord-f587de205fb14fe18c0c8de2e5dbd414
- 出典データセット
- uspto-grants-1981_07
- 特許番号
- US04279887
関連ノート
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