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Sulfuric Acid → 2,5-Difluorobenzaldehyde

HRID 3968
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HRID 3968 반응식
[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]
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참가 물질

6

반응물 4

HCID 1118Sulfuric AcidHCID 108921,4-DifluorobenzeneHCID 66737N-MethylformanilideHCID 178418339Butyllithium

생성물 1

HCID 1376632,5-Difluorobenzaldehyde수율 77.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
-60 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-83db2d9a2e8647bebb243a700d6a3748
출처 데이터셋
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04723009

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