Hydrochloric Acid → Methyl 4-methylnaphthalene-1-carboxylate
反応式
[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([C:12]([OH:14])=[O:13])=[CH:4][CH:3]=1.Cl.[CH3:16]O>>[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([C:12]([O:14][CH3:16])=[O:13])=[CH:4][CH:3]=1参加物
4
実験手順
Commercially available 4-methyl-1-naphthalenecarboxylic acid (250.6 mg) was dissolved in methanol (7.5 ml). Hydrogen chloride gas was blown into the solution for five minutes while cooling with ice. Then, the mixture was stirred for 19 hours at room temperature and the solvent was removed by distillation. The residue was dissolved in chloroform, washed with 1 mol/l aqueous solution of sodium hydroxide, and dried over anhydrous sodium sulfate. The solvent was removed by distillation. The residue was dried under reduced pressure to obtain the target compound (269.9 mg) as colorless oil.
後処理
- temperaturewhile cooling with ice
- customthe solvent was removed by distillation
- dissolutionThe residue was dissolved in chloroform
- washwashed with 1 mol/l aqueous solution of sodium hydroxide
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was removed by distillation
- customThe residue was dried under reduced pressure
出典と根拠
- ORDレコード
- ord-b8d808e82a4642758ddd699886c22acc
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07098215B2
反応ノート
読み込み中…