2,3-Dimethylphenol → Xibenolol
反応式
[C:1]([N:5]1[CH2:8][CH:7]([OH:9])[CH2:6]1)([CH3:4])([CH3:3])[CH3:2].[C:10]1([OH:18])[CH:15]=[CH:14][CH:13]=[C:12]([CH3:16])[C:11]=1[CH3:17].[OH-].[K+]>CCOCC>[CH3:17][C:11]1[C:12]([CH3:16])=[CH:13][CH:14]=[CH:15][C:10]=1[O:18][CH2:6][CH:7]([OH:9])[CH2:8][NH:5][C:1]([CH3:2])([CH3:3])[CH3:4]参加物
反応条件
- 温度
- 155 °C
実験手順
To a mixture of 6.5 parts of 1-(tert.-butyl)-3-azetidinol and 6.7 parts of 2,3-xylenol 0.2 part of potassium hydroxide was added, and the mixture was heated at 155° C. for 20 hours. The reaction mixture was cooled and then dissolved in 100 parts of ether. The solution was washed three times with 50 parts of 2N-sodium hydroxide aqueous solution and extracted three times with 2N-hydrochloric acid aqueous solution. The extract was washed with 50 parts of ether and was made alkaline by adding 2N-sodium hydroxide solution gradually thereto. Then, the ether extraction was conducted three times and the extract was condensed and allowed to stand in a cool place. As a result crystals were formed, which were recrystallized twice from ether to yield 8.3 parts of 1-(2',3'-dimethylphenyloxy)-3-(tert.-butylamino)-2-propanol having a melting point of 57° C. Results of infra-red spectrum analysis and ultraviolet ray absorption analysis of the product are as follows:
後処理
- additionwas added
- temperatureThe reaction mixture was cooled
- washThe solution was washed three times with 50 parts of 2N-sodium hydroxide aqueous solution
- extractionextracted three times with 2N-hydrochloric acid aqueous solution
- washThe extract was washed with 50 parts of ether
- additionby adding 2N-sodium hydroxide solution gradually
- extractionThen, the ether extraction
- customcondensed
- customAs a result crystals were formed
- customwhich were recrystallized twice from ether
出典と根拠
- ORDレコード
- ord-ea1fad422f424c9cbbaeb0564efd0ab2
- 出典データセット
- uspto-grants-1977_04
- 特許番号
- US04018824
反応ノート
読み込み中…