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Water → Ethyl 4-azido-2-fluoro-3-methylbenzoate

HRID 377273
ノート
印刷プレビュー

反応式

HRID 377273 の反応式
[F:1][C:2]1[C:12]([CH3:13])=[C:11](F)[CH:10]=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5].[N-:15]=[N+:16]=[N-:17].[Na+].C1(C)C=CC=CC=1.O>CS(C)=O>[N:15]([C:11]1[CH:10]=[CH:9][C:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])=[C:2]([F:1])[C:12]=1[CH3:13])=[N+:16]=[N-:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 1140TolueneHCID 33557Sodium AzideHCID 19358331Ethyl 2,4-difluoro-3-methylbenzoate

生成物 1

HCID 19358340Ethyl 4-azido-2-fluoro-3-methylbenzoate収率 42.4%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

In 47 ml of dimethyl sulfoxide was dissolved 4.65 g of ethyl 2,4-difluoro-3-methylbenzoate, followed by adding thereto 3.32 g of sodium azide, and the resulting mixture was stirred at 70° C. for 20 hours. The reaction mixture was cooled to room temperature and then added to a mixed solvent of 150 ml of toluene and 150 ml of water, and the organic layer was separated. The organic layer obtained was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The resulting residue was purified by a column chromatography (eluent: toluene) to obtain 2.20 g of ethyl 4-azido-2-fluoro-3-methylbenzoate as a light-yellow oil.

後処理

  1. additionby adding
  2. customthe organic layer was separated
  3. customThe organic layer obtained
  4. washwas washed with water
  5. dry with materiala saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
  6. distillationdistilled under reduced pressure
  7. customto remove the solvent
  8. customThe resulting residue was purified by a column chromatography (eluent: toluene)

出典と根拠

ORDレコード
ord-9a77eb6135e640e58217b98678ef6a41
出典データセット
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06025370

反応ノート

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