2,3-Dimethylphenol → Xibenolol
반응식
[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]참가 물질
반응 조건
- 온도
- 155 °C
실험 절차
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 2 N-sodium hydroxide aqueous solution and extracted three times with 2 N-hydrochloric acid aqueous solution. The extract was washed with 50 parts of ether and was made alkaline by adding 2 N-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:
후처리
- additionwas added
- temperatureThe reaction mixture was cooled
- washThe solution was washed three times with 50 parts of 2 N-sodium hydroxide aqueous solution
- extractionextracted three times with 2 N-hydrochloric acid aqueous solution
- washThe extract was washed with 50 parts of ether
- additionby adding 2 N-sodium hydroxide solution gradually
- extractionThen, the ether extraction
- customcondensed
- customAs a result, crystals were formed which
- customwere recrystallized twice from ether
출처 및 근거
- ORD 기록
- ord-4ba1891598db49a6ace2d51d0759f563
- 출처 데이터셋
- uspto-grants-1982_11
- 특허 번호
- US04360464
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