反応式
Cl.Cl[CH2:3][C:4]1[CH:13]=[CH:12][C:11]([OH:14])=[C:10]2[C:5]=1[CH:6]=[CH:7][CH:8]=[N:9]2.[CH3:15][O-:16].[Na+]>CO>[CH3:15][O:16][CH2:3][C:4]1[CH:13]=[CH:12][C:11]([OH:14])=[C:10]2[C:5]=1[CH:6]=[CH:7][CH:8]=[N:9]2参加物
4
実験手順
5-Chloromethyl-8-hydroxyquinoline hydrochloride (2.145 g; 9.3 mmol) was added to a mixture of sodium methoxide (1.763 g; 32.6 mmol) in MeOH (40 ml). The reaction mixture was stirred for about 4 h at room temperature, and then evaporated to dryness. The residue was dissolved in CHCl3 (100 ml, the solution was washed with water until a neutral pH was obtained, and was then washed with brine, dried over Na2SO4 and evaporated to dryness. The residue was extracted with hexane (100 ml). The hexane solution was evaporated to give the title product, 0.36 g (20%). M.p. 75-760° C. TLC (CHCl3/MeOH/NH3.9.5:0.5:0.1). Rf=0.36.
後処理
- customevaporated to dryness
- dissolutionThe residue was dissolved in CHCl3 (100 ml
- washthe solution was washed with water until a neutral pH
- customwas obtained
- washwas then washed with brine
- dry with materialdried over Na2SO4
- customevaporated to dryness
- extractionThe residue was extracted with hexane (100 ml)
- customThe hexane solution was evaporated
出典と根拠
- ORDレコード
- ord-2ec5d463dceb4791969bf473db271151
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06855711B1
関連ノート
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