Nitric Acid → 2,6-Difluoro-3-nitrotoluene
反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[CH3:9].[N+:10]([O-])([OH:12])=[O:11]>OS(O)(=O)=O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([N+:10]([O-:12])=[O:11])=[C:4]([F:8])[C:3]=1[CH3:9]参加物
4
実験手順
A solution of 1,3-difluoro-2-methylbenzene (15 g, 0.12 mol) in H2SO4 (100 mL) was treated dropwise with HNO3 (65%, 11.4 g, 0.12 mol) at −10° C. The resultant mixture was stirred for about 30 min. The mixture was poured into ice-water and extracted with EtOAc (3×200 mL). The combined organics were washed with brine, dried (NaSO4) and concentrated in vacuo to give 1,3-difluoro-2-methyl-4-nitrobenzene (16 g, 78% yield). 1H NMR (400 MHz, CDCl3) δ 7.80 (m, 1H), 6.8-7.1 (m, 1H), 2.30 (s, 3H).
後処理
- extractionextracted with EtOAc (3×200 mL)
- washThe combined organics were washed with brine
- dry with materialdried (NaSO4)
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-a23e453c7d0544d3953cfdb6d9edb610
- 出典データセット
- uspto-grants-2010_09
- 特許番号
- US07790756B2
反応ノート
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