Water → 1-benzyl-5-(1-hydroxy-4,4-diphenylbutyl)-1H-imidazole
反応式
[Mg].Br[CH2:3][CH2:4][CH:5]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[CH2:18]([N:25]1[C:29]([CH:30]=[O:31])=[CH:28][N:27]=[CH:26]1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.O>O1CCCC1>[CH2:18]([N:25]1[C:29]([CH:30]([OH:31])[CH2:3][CH2:4][CH:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)=[CH:28][N:27]=[CH:26]1)[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1参加物
実験手順
2,0 g of magnesium turnings are covered with 60 ml of dry tetrahydrofuran. To the mixture is then added dropwise a solution of 1-bromo-3,3-diphenylpropane (22,9 g) in 20 ml of dry tetrahydrofuran at such a rate that a smooth reaction is maintained. After the addition is complete, the reaction mixture is refluxed for one additional hour and cooled to room temperature. The reaction mixture is then added dropwise to a solution of 1-benzyl-5-imidazolecarbaldehyde (7,35 g) in 80 ml of tetrahydrofuran at 60° C. After the addition is complete, the reaction mixture is refluxed for 2 hours, cooled and poured into cold water. Tetrahydrofuran is evaporated and to the solution is added conc. hydrochloric acid. The solution is cooled and the precipitate which contains the product as hydrochloride salt is removed by filtration, washed with water and dried. Yield 14,1 g. M.p. 160°-168° C.
後処理
- customthat a smooth reaction
- temperatureis maintained
- additionAfter the addition
- temperaturethe reaction mixture is refluxed for one additional hour
- additionAfter the addition
- temperaturethe reaction mixture is refluxed for 2 hours
- temperaturecooled
- customTetrahydrofuran is evaporated and to the solution
- additionis added conc. hydrochloric acid
- temperatureThe solution is cooled
- customis removed by filtration
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-6d3ff6c475b2462dacf6425b90b7297c
- 出典データセット
- uspto-grants-1995_08
- 特許番号
- US05439928
反応ノート
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