Hydrogen Bromide → 4-Bromo-2-fluoro-3-methylbenzoic acid

HRID 377276ノート

反応式

HRID 377276 の反応式
N[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([F:11])[C:3]=1[CH3:12].N([O-])=O.[Na+].C1(C)C=CC=CC=1.[BrH:24]>O>[Br:24][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([F:11])[C:3]=1[CH3:12]

参加物

6

反応物 4

HCID 260Hydrogen BromideHCID 1140TolueneHCID 193583204-Amino-2-fluoro-3-methylbenzoic acidHCID 23668193Sodium Nitrite

生成物 1

HCID 193583684-Bromo-2-fluoro-3-methylbenzoic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

In 14 ml of 4.7% hydrobromic acid was suspended 0.55 g of 4-amino-2-fluoro-3-methylbenzoic acid, and 3.7 g of cupric bromide was added thereto. To the resulting suspension was added dropwise a solution of 0.38 g of sodium nitrite in 4 ml of water under ice-cooling over a period of 15 minutes, and the resulting mixture was stirred at the same temperature for 1 hour and then at room temperature for 24 hours. To the reaction mixture was added 20 ml of toluene and the organic layer was separated. The organic layer obtained was washed with 20 ml of 20% hydrobromic acid, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. n-Hexane was added to the resulting residue and the crystals were collected by filtration to obtain 0.68 g of colorless 4-bromo-2-fluoro-3-methylbenzoic acid.

後処理

  1. additionwas added
  2. temperaturecooling over a period of 15 minutes
  3. waitat room temperature for 24 hours
  4. customthe organic layer was separated
  5. customThe organic layer obtained
  6. washwas washed with 20 ml of 20% hydrobromic acid
  7. dry with materialdried over anhydrous magnesium sulfate
  8. distillationdistilled under reduced pressure
  9. customto remove the solvent
  10. additionn-Hexane was added to the resulting residue
  11. filtrationthe crystals were collected by filtration

出典と根拠

ORDレコード
ord-04b1187993e34da0b560970321a2e046
出典データセット
uspto-grants-2000_02
特許番号
US06025370

反応ノート

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