Hydrochloric Acid → 5-Bromo-2-methoxy-3-methylbenzoic acid
反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH3:14])[C:5]([O:12][CH3:13])=[C:6]([CH:11]=1)[C:7]([O:9]C)=[O:8].[OH-].[Na+].O.Cl>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH3:14])[C:5]([O:12][CH3:13])=[C:6]([CH:11]=1)[C:7]([OH:9])=[O:8]参加物
6
実験手順
To a solution of methyl 5-bromo-2-methoxy-3-methyl-benzoate (2.6 g, 10.0 mmol, 1.0 eq) in THF (20 mL) was added an aqueous solution of NaOH (2M, 20 mL, 40 mmol, 4.0 eq). The mixture was stirred at room temperature for 5 h. Water was added and the aqueous layer was acidified to pH 9 by addition of 1M HCl. The THF was removed in vacuo and the aqueous layer was further acidified to pH 4-5 with 1M HCl. The solid that precipitated from the reaction was collected by filtration and dried to give the title compound as a white solid (1.8 g, 73%).
後処理
- customThe THF was removed in vacuo
- customThe solid that precipitated from the reaction
- filtrationwas collected by filtration
- customdried
出典と根拠
- ORDレコード
- ord-c47194d446964f7cb9ee6b669610bc9f
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09249085B2
反応ノート
読み込み中…