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Chlorosuccinimide → 4-Chloro-2,3-difluoro-6-nitroaniline

HRID 2227185
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HRID 2227185 반응식
[F:1][C:2]1[C:8]([F:9])=[CH:7][CH:6]=[C:5]([N+:10]([O-:12])=[O:11])[C:3]=1[NH2:4].[Cl:13]N1C(=O)CCC1=O>CN(C)C=O>[Cl:13][C:7]1[CH:6]=[C:5]([N+:10]([O-:12])=[O:11])[C:3]([NH2:4])=[C:2]([F:1])[C:8]=1[F:9]
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 27370282,3-Difluoro-6-nitroaniline

생성물 1

HCID 178973294-Chloro-2,3-difluoro-6-nitroaniline

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
85 °C

실험 절차

2,3-Difluoro-6-nitroaniline (15.4 g, 88.7 mmol), N-chlorosuccinimide (14.9 g, 111.4 mmol) and N,N-dimethylformamide (250 mL) were combined and were heated to 80-90° C. for several hours, after which time the mixture was poured into ice water. The product was extracted with ethyl acetate which was then washed with water, saturated aqueous sodium chloride, dried over magnesium sulfate, filtered and the solvents were removed in vacuo to leave a yellow, viscous oil. 1H NMR (DMSO-d6) δ: 8.03 (dd, J=7.3, 2.2 Hz, 1H, Ar—H), 7.65 (br s, 2H, NH2).

후처리

  1. extractionThe product was extracted with ethyl acetate which
  2. washwas then washed with water, saturated aqueous sodium chloride
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. customthe solvents were removed in vacuo
  6. customto leave a yellow, viscous oil

출처 및 근거

ORD 기록
ord-482413f54be44b608a4a9dfcb7b81063
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06413938B1

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