Hydrochloric Acid → HCID 19862550、化合物
反応式
[OH:1][C:2]1[C:15]([C:16]([CH3:19])([CH3:18])[CH3:17])=[CH:14][C:5]([CH:6]=[N:7][N:8]2[CH:12]=[C:11]([CH3:13])[N:10]=[CH:9]2)=[CH:4][C:3]=1[C:20]([CH3:23])([CH3:22])[CH3:21].Cl.O.[H][H]>CO.[C].[Pd]>[OH:1][C:2]1[C:15]([C:16]([CH3:18])([CH3:17])[CH3:19])=[CH:14][C:5]([CH2:6][NH:7][N:8]2[CH:12]=[C:11]([CH3:13])[N:10]=[CH:9]2)=[CH:4][C:3]=1[C:20]([CH3:23])([CH3:22])[CH3:21]参加物
実験手順
6.1 g of 1-(4-hydroxy-3,5-di-tert.-butylbenzylideneamino)-4-methylimidazole are hydrogenated at normal pressure and room temperature in 100 ml of methanol, 21 ml of 1N hydrochloric acid and 30 ml of water in the presence of palladium-carbon. After 500 ml of hydrogen have been taken up, the mixture is filtered. The filtrate is evaporated to a volume of 50 ml. Then, 50 ml of water are added and the mixture is treated with saturated sodium bicarbonate solution up to a neutral reaction (pH=7). The separated crystals are removed by filtration, and taken up with methylene chloride. The methylene chloride solution is washed once with water, dried and evaporated. The residue is triturated with cold ether. Thereafter the solid is removed by filtration, washed with ether and n-hexane and dried at 60° in a vacuum. There is obtained 1-(4-hydroxy-3,5-di-tert.-butylbenzylamino)-4-methylimidazole of m.p. 150°-151°.
後処理
- filtrationthe mixture is filtered
- customThe filtrate is evaporated to a volume of 50 ml
- additionThen, 50 ml of water are added
- additionthe mixture is treated with saturated sodium bicarbonate solution up to a neutral reaction (pH=7)
- customThe separated crystals are removed by filtration
- washThe methylene chloride solution is washed once with water
- customdried
- customevaporated
- customThe residue is triturated with cold ether
- customThereafter the solid is removed by filtration
- washwashed with ether and n-hexane
- customdried at 60° in a vacuum
出典と根拠
- ORDレコード
- ord-e938ab1951134e8a9a505a4a6c032f3e
- 出典データセット
- uspto-grants-1990_03
- 特許番号
- US04908363
反応ノート
読み込み中…