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1-Chloro-4,5-difluoro-2-nitrobenzene → 1-Chloro-4-fluoro-5-methoxy-2-nitrobenzene

HRID 1831488
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HRID 1831488 반응식
[CH3:1][O-:2].[Na+].[Cl:4][C:5]1[CH:10]=[C:9](F)[C:8]([F:12])=[CH:7][C:6]=1[N+:13]([O-:15])=[O:14]>CO>[Cl:4][C:5]1[CH:10]=[C:9]([O:2][CH3:1])[C:8]([F:12])=[CH:7][C:6]=1[N+:13]([O-:15])=[O:14]
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참가 물질

4

반응물 2

HCID 101303301-Chloro-4,5-difluoro-2-nitrobenzeneHCID 10942334Sodium Methoxide

생성물 1

HCID 220520461-Chloro-4-fluoro-5-methoxy-2-nitrobenzene수율 79%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To sodium methoxide (100 mL of a 0.5 M solution in methanol, 50.1 mmol) cooled to 0° C. was added a solution of 1-chloro-4,5-difluoro-2-nitro-benzene (9.7 g, 50.1 mmol) in methanol (10 mL) dropwise over 15 min. The solution was warmed to room temperature and stirred for 2 h, then poured slowly over ice. The yellow precipitate was collected by filtration and washed with cold water. The crystals were air dried to give 8.2 g (79%) of 1-chloro-4-fluoro-5-methoxy-2-nitro-benzene: Crude 1H NMR (400 MHz, CDCl3): δ 7.85 (d, J=10.5 Hz, 1H), 7.06 (d, J=7.3 Hz, 1H), 3.98 (s, 3H). The crude material was pure enough to carry on to the next step.

후처리

  1. additionpoured slowly over ice
  2. filtrationThe yellow precipitate was collected by filtration
  3. washwashed with cold water
  4. customdried

출처 및 근거

ORD 기록
ord-4dd41c78ea384e31bf3dfac737e75869
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067658B2

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