Ammonium Hydroxide → 4-Fluoro-2-hydroxybenzamide
反応式
[F:1][C:2]1[CH:3]=[C:4]([OH:11])[C:5](=[CH:9][CH:10]=1)[C:6](O)=[O:7].C(Cl)(=O)C(Cl)=O.[OH-].[NH4+:19]>CN(C=O)C.C1COCC1>[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:19])=[O:7])=[C:4]([OH:11])[CH:3]=1参加物
6
実験手順
DMF (2 drops) was added to a mixture of 4-fluorosalicylic acid (5 g, 32.0 mmol) and oxalyl chloride (7.11 mL, 80.1 mmol) in THF (35 mL). The mixture was stirred for 2 hours then reduced in vacuo. The residue was dissolved in THF (20 mL) and added dropwise to concentrated ammonium hydroxide solution (30 mL) at 0° C. The reaction was stirred at RT for 20 hours and the THF removed in vacuo. The residue was acidified and a white solid was filtered off. The solid was dissolved in ethyl acetate (80 mL) and the solution washed with water (50 mL), saturated sodium bicarbonate solution (50 mL), dried (MgSO4), and reduced in vacuo to give the desired compound as a yellow solid (2.4 g).
後処理
- stirringThe reaction was stirred at RT for 20 hours
- customthe THF removed in vacuo
- filtrationa white solid was filtered off
- dissolutionThe solid was dissolved in ethyl acetate (80 mL)
- washthe solution washed with water (50 mL), saturated sodium bicarbonate solution (50 mL)
- dry with materialdried (MgSO4)
出典と根拠
- ORDレコード
- ord-b5173b59ffe647c3874af25244d27cca
- 出典データセット
- uspto-grants-2011_05
- 特許番号
- US07943607B2
反応ノート
読み込み中…