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Bromine → 2-Bromo-6-fluoro-4-nitrotoluene

HRID 1417529
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HRID 1417529 반응식
[F:1][C:2]1[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[CH:5]=[CH:6][C:7]=1[CH3:8].[Br:12]Br>[Fe]>[Br:12][C:6]1[CH:5]=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=[C:2]([F:1])[C:7]=1[CH3:8]
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참가 물질

4

반응물 2

HCID 24408BromineHCID 740252-Fluoro-4-nitrotoluene

생성물 1

HCID 542079842-Bromo-6-fluoro-4-nitrotoluene수율 23.2%

시약·촉매·용매 1

HCID 23925Iron촉매

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온도
100 °C

실험 절차

To 3-fluoro-4-methylnitrobenzene (4.0 gm, 25.8 mmol) was added bromine (5.2 gm, 32 mmol) and iron powder (100 mg). The mixture was heated under a condenser at 100° C. for 40 hr and then poured into ice water containing enough sodium sulfite to quench the excess bromine. The aqueous layer was extracted twice with ether and the ether layers were washed with brine, dried over sodium sulfate, combined and evaporated. The residue was purified by FC (10-20% ethyl acetate/hexanes) to afford 1.4 gm of the title compound as a white solid (the major and highest Rf isomer). NMR (CDCl3): δ 2.41 (d, 3H, J=3 Hz), 7.85 (dd, 1H, J=2.1 and 9 Hz), 8.24 (dd, 1H, J=1.8 and 2.1 Hz).

후처리

  1. customto quench the excess bromine
  2. extractionThe aqueous layer was extracted twice with ether
  3. washthe ether layers were washed with brine
  4. dry with materialdried over sodium sulfate
  5. customevaporated
  6. customThe residue was purified by FC (10-20% ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-a24ccd3afe1d4fa38495de182ef3a319
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05877191

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