반응식
[CH3:1][N:2]([CH3:11])[CH2:3][CH2:4][C:5]1[CH2:10][CH:9]=CC[CH:6]=1.[C:12]([OH:15])(=O)[CH3:13].II.C(OCC)(=[O:20])C>C([O-])(=O)C.[Ag+]>[CH3:1][N:2]([CH3:11])[CH2:3][CH2:4][C:5]1[CH2:10][C@@H:9]([OH:20])[C@H:12]([OH:15])[CH2:13][CH:6]=1참가 물질
실험 절차
A solution of 45 g. (0.3 moles) of 1-[2-(dimethylamino)-ethyl]-1,4-cyclohexadiene from Example 3(a) in 1.5 l. of dry glacial acetic acid is treated with 100 g. of silver acetate and 75 g. of iodine. The mixture is stirred until most of the iodine dissolves and is then heated for two hours at 95°. The reaction solution is cooled, filtered and evaporated in vacuo to give an oil. The oil is taken up in ethyl acetate and washed with aqueous sodium bicarbonate solution. The organic phase is dried (MgSO4) and evaporated to an oil. The oil is taken up in ethyl acetate and treated with HCl in isopropanol. The resulting crude solid is removed by filtration and recrystallized from acetonitrile-ether to yield dl-trans-4-[2-(dimethylamino)-ethyl]-4-cyclohexene-1,2-diol, diacetate ester, hydrochloride salt.
후처리
- dissolutiondissolves
- temperatureis then heated for two hours at 95°
- temperatureThe reaction solution is cooled
- filtrationfiltered
- customevaporated in vacuo
- customto give an oil
- washwashed with aqueous sodium bicarbonate solution
- dry with materialThe organic phase is dried (MgSO4)
- customevaporated to an oil
- additiontreated with HCl in isopropanol
- customThe resulting crude solid is removed by filtration
- customrecrystallized from acetonitrile-ether
출처 및 근거
- ORD 기록
- ord-b120cb378f7d474b876bc775b36ea058
- 출처 데이터셋
- uspto-grants-1978_12
- 특허 번호
- US04131744
연결된 노트
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