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N-bromobutanimide → 5-Bromo-2,3-difluorobenzaldehyde

HRID 1057131
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HRID 1057131 반응식
[F:1][C:2]1[C:9]([F:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].C1C(=O)N([Br:18])C(=O)C1>OS(O)(=O)=O>[Br:18][C:7]1[CH:8]=[C:9]([F:10])[C:2]([F:1])=[C:3]([CH:6]=1)[CH:4]=[O:5]
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 1376642,3-Difluorobenzaldehyde

생성물 1

HCID 230701825-Bromo-2,3-difluorobenzaldehyde수율 26.6%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

To a solution of 2,3-difluorobenzaldehyde (42 g, 0.296 mol) in H2SO4 (150 mL), was added NBS (63 g, 0.354 mol) in three portions over a period of 30 minutes at 60° C. The resulting mixture was heated for 6 hours at this temperature under N2. Work-up: the reaction mixture was poured into ice water. Petroleum ether (300 mL) was added, and the mixture was stirred for 10 minutes. The organic layer was separated, and the aqueous layer was extracted with more petroleum ether (300 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on silica gel (0˜0.5% EtOAc in petroleum ether) to give 5-bromo-2,3-difluorobenzaldehyde (17.4 g). 1H NMR (300 MHz, CDCl3): δ 10.32 (s, 1H), 7.81-7.79 (m, 1H), 7.65-7.60 (m, 1H).

후처리

  1. temperatureThe resulting mixture was heated for 6 hours at this temperature under N2
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with more petroleum ether (300 mL)
  4. dry with materialThe combined organic layers were dried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by column chromatography on silica gel (0˜0.5% EtOAc in petroleum ether)

출처 및 근거

ORD 기록
ord-31e9c398423641359a9e37db3ef08230
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09399646B2

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