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Formic Acid → 4-Amino-3-bromo-2,5-difluorobenzaldehyde

HRID 595020
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HRID 595020 반응식
[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:5]([C:6]#N)=[C:4]([F:11])[C:3]=1[Br:12].C(O)=[O:14]>[Ni]>[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:5]([CH:6]=[O:14])=[C:4]([F:11])[C:3]=1[Br:12]
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참가 물질

4

반응물 2

HCID 284Formic AcidHCID 146210194-Amino-3-bromo-2,5-difluorobenzonitrile

생성물 1

HCID 146210204-Amino-3-bromo-2,5-difluorobenzaldehyde수율 83%

시약·촉매·용매 1

HCID 935Nickel촉매

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온도
85 °C

실험 절차

Raney nickel (5.3 g, 50% slurry in water) was added to a solution of 4-amino-3-bromo-2,5-difluoro-benzonitrile (4.0 g, 17.2 mmol) in formic acid (60 mL). After heating for 1 h at 85° C., the reaction mixture was filtered through Celite, washed with DCM and evaporated to dryness. The residue was suspended in DCM and neutralized carefully with saturated sodium hydrogencarbonate. The aqueous phase was extracted with DCM and the combined organic phases were dried over sodium sulfate and evaporated to yield 4-amino-3-bromo-2,5-difluorobenzaldehyde (3.4 g, 14.3 mmol, 83%). 1H NMR (d6-DMSO) δ 9.91 (d, J=3.0 Hz, 1H), 7.45 (dd, J=11.0, 6.0 Hz, 1H), 6.96 (br s, 2H).

후처리

  1. filtrationthe reaction mixture was filtered through Celite
  2. washwashed with DCM
  3. customevaporated to dryness
  4. extractionThe aqueous phase was extracted with DCM
  5. dry with materialthe combined organic phases were dried over sodium sulfate
  6. customevaporated

출처 및 근거

ORD 기록
ord-c2b821d083ec4d0d8472be6ae05764ba
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242987B2

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