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Sulfuric Acid → 2,5-Difluorobenzaldehyde

HRID 3968
ノート
印刷プレビュー

反応式

HRID 3968 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][CH:3]=1.C([Li])CCC.CN([CH:22]=[O:23])C1C=CC=CC=1.S(=O)(=O)(O)O>O1CCCC1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH:22]=[O:23]
参加物反応条件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 1118Sulfuric AcidHCID 108921,4-DifluorobenzeneHCID 66737N-MethylformanilideHCID 178418339Butyllithium

生成物 1

HCID 1376632,5-Difluorobenzaldehyde収率 77.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-60 °C

実験手順

To a stirred solution of 194.5 g (1.70 mol) of 1,4-difluorobenzene in 2 of dry tetrahydrofuran at -60° C. was added dropwise over 45 mins 1.70 mol (2.2 M in hexane) of n-butyllithium at a rate such that the temperature remained below -55° C. The reaction mixture was stirred for 45 mins at below -50° C. and 1.5 hr at -50° to -45° C. The solution was then cooled to -60° C. and a solution to 230 g of N-methylformanilide in 300 ml of tetrahydrofuran was added dropwise over 30 mins. The mixture was stirred for 1 hr at -50° C. and allowed to warm to -30° C. over 15 mins. The mixture was then poured into ice water, neutralized (pH 6-7) with 10% sulfuric acid and extracted three times with hexane. The extracts were washed once with 1N sulfuric acid, once with saturated sodium chloride solution and concentrated to an oil. Distillation at 64°-65° C. (20 mm) provided 187.5 g (77.5%) of product.

後処理

  1. customremained below -55° C
  2. stirringThe mixture was stirred for 1 hr at -50° C.
  3. temperatureto warm to -30° C. over 15 mins
  4. extractionextracted three times with hexane
  5. washThe extracts were washed once with 1N sulfuric acid, once with saturated sodium chloride solution
  6. concentrationconcentrated to an oil
  7. distillationDistillation at 64°-65° C. (20 mm)

出典と根拠

ORDレコード
ord-83db2d9a2e8647bebb243a700d6a3748
出典データセット
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04723009

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート