Methanol → Benzoic acid, 3,4-dihydroxy-5-nitro-, methyl ester
反応式
S(Cl)(Cl)=O.[OH:5][C:6]1[CH:7]=[C:8]([CH:12]=[C:13]([N+:16]([O-:18])=[O:17])[C:14]=1[OH:15])[C:9]([OH:11])=[O:10].[CH3:19]O>>[OH:5][C:6]1[CH:7]=[C:8]([CH:12]=[C:13]([N+:16]([O-:18])=[O:17])[C:14]=1[OH:15])[C:9]([O:11][CH3:19])=[O:10]参加物
4
実験手順
Thionyl chloride (6.07 mL, 83 mmol) was added drop wise to a stirred solution of 3,4-dihydroxy-5-nitrobenzoic acid (14.4 g, 72.3 mmol) in MeOH (70 mL) at room temperature for 1 h. The reaction mixture was refluxed for 3 h and concentrated. The residue was recrystallized from water and vacuum-dried to afford the desired ester (11.0 g, 51.6 mmol, 71.4% yield).
後処理
- temperatureThe reaction mixture was refluxed for 3 h
- concentrationconcentrated
- customThe residue was recrystallized from water
- customvacuum-dried
出典と根拠
- ORDレコード
- ord-dc7982a5252b4d51976a00c7acb0220b
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08119624B2
反応ノート
読み込み中…