Benzyl Bromide → HCID 66868184、化合物
反応式
[H-].[Na+].[CH3:3][O:4][C:5]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[CH:7][C:6]=1[CH2:13][CH2:14][CH2:15][OH:16].[CH2:17](Br)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>C1COCC1>[CH2:17]([O:16][CH2:15][CH2:14][CH2:13][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]([O:11][CH3:12])[C:5]=1[O:4][CH3:3])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1参加物
実験手順
2.50 g (62.5 mmol) NaH (60% in oil) were suspended under nitrogen in 70 ml dry THF and a solution of 7.1 g (36.2 mmol) 3-(2,3-dimethoxy-phenyl)-propan-1-ol (J. Org. Chem., 1987, 52, 1072) in 50 ml THF was added dropwise at 18° C. The resulting mixture was stirred for 30 minutes and then a solution of 6.81 g (39.8 mmol) benzylbromide in 30 ml THF was added dropwise and the mixture was stirred over night at 18° C. The reaction was quenched with 10 ml water and the organic solvent was evaporated under reduced pressure. The residue was dissolved in 200 ml of ethyl acetate and the organic layer was washed with water and brine, dried over Na2SO4 and evaporated in vacuo. The crude product was purified by column chromatography on silica gel (ethyl acetate/n-hexane 1:40) to afford 8 g (77%) of the desired product as a colorless oil.
後処理
- stirringthe mixture was stirred over night at 18° C
- customThe reaction was quenched with 10 ml water
- customthe organic solvent was evaporated under reduced pressure
- dissolutionThe residue was dissolved in 200 ml of ethyl acetate
- washthe organic layer was washed with water and brine
- dry with materialdried over Na2SO4
- customevaporated in vacuo
- customThe crude product was purified by column chromatography on silica gel (ethyl acetate/n-hexane 1:40)
出典と根拠
- ORDレコード
- ord-b3a307a5adea4d67badb37cb455f854a
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08173609B2
反応ノート
読み込み中…