Potassium Carbonate → Acifluorfen-methyl

HRID 128484

反応式

HRID 128484 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1[OH:12].C(=O)([O-])[O-].[K+].[K+].F[C:20]1[CH:21]=[CH:22][C:23]([N+:30]([O-:32])=[O:31])=[C:24]([CH:29]=1)[C:25]([O:27][CH3:28])=[O:26]>CS(C)=O>[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:10])([F:11])[F:9])[CH:5]=[CH:4][C:3]=1[O:12][C:20]1[CH:21]=[CH:22][C:23]([N+:30]([O-:32])=[O:31])=[C:24]([CH:29]=1)[C:25]([O:27][CH3:28])=[O:26]

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 27366032-Chloro-4-(trifluoromethyl)phenolHCID 51520495-Fluoro-2-nitrobenzoic acid methyl ester

生成物 1

HCID 91642Acifluorfen-methyl収率 84%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

To a 5-liter, 4-necked flask fitted with a stirrer, thermometer, addition funnel, reflux condenser and drying tube is added dimethyl sulfoxide (200 ml), 2-chloro-4-trifluoromethylphenol) (715 g, 3.64 mole), and anhydrous potassium carbonate (520 g, 3.72 moles). The reaction mixture is stirred at room temperature overnight under a nitrogen atmosphere. Then methyl 5-fluoro-2-nitrobenzoate (724 g, 3.64 moles) is added over a 1 hour period (slight exotherm to 31° C.). After stirring overnight at room temperature, the inorganic solids are removed by filtration and 1700 ml of dimethyl sulfoxide removed under vacuum (1 mm, pot temp. of 85° C., vapor temp. of -40° C.). The residue is diluted with a large volume of carbon tetrachloride and water washed. The organic layer is dried with anhydrous magnesium sulfate and the solvent removed under vacuum to afford 1142 g of methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate (84% yield). Anal. Calcd. for C15H9ClF3NO5 : C, 47.90; H, 2.42; Cl, 9.45; F, 15.20; N, 3.73. Found: C, 47.83; H, 2.47; Cl, 9.15; L F, 14.84; N, 3.69.

後処理

  1. customTo a 5-liter, 4-necked flask fitted with a stirrer
  2. additionthermometer, addition funnel
  3. temperaturereflux condenser
  4. customdrying tube
  5. stirringAfter stirring overnight at room temperature
  6. customthe inorganic solids are removed by filtration and 1700 ml of dimethyl sulfoxide
  7. customremoved under vacuum (1 mm, pot temp. of 85° C., vapor temp. of -40° C.)
  8. additionThe residue is diluted with a large volume of carbon tetrachloride and water
  9. washwashed
  10. dry with materialThe organic layer is dried with anhydrous magnesium sulfate
  11. customthe solvent removed under vacuum

出典と根拠

ORDレコード
ord-7d47697a8a054a53b36c6a9edd237aff
出典データセット
uspto-grants-1981_03
特許番号
US04259510

関連ノート

読み込み中…