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Methyl iodide → 5-Bromo-1,2-dimethyl-3-nitrobenzene

HRID 2208681
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인쇄 미리보기

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HRID 2208681 반응식
[Br:1][C:2]1[CH:3]=[C:4]([N+:12]([O-:14])=[O:13])[C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7](O)=O.C(=O)([O-])[O-].[Na+].[Na+].CI>CN(C=O)C>[CH3:7][C:6]1[CH:10]=[C:2]([Br:1])[CH:3]=[C:4]([N+:12]([O-:14])=[O:13])[C:5]=1[CH3:11]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 10340Sodium CarbonateHCID 137700085-Bromo-2-methyl-3-nitrobenzoic acid

생성물 1

HCID 123818655-Bromo-1,2-dimethyl-3-nitrobenzene수율 119%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
60 °C

실험 절차

To a stirred solution of 5-bromo-2-methyl-3-nitrobenzoic acid (287 g, 1103 mmol) in DMF (150 mL), sodium carbonate (468 g, 4415 mmol) and methyl iodide (626.63 g, 4415 mmol) were added. Resulting reaction mass was heated at 60° C. for 8 h. On completion, solid precipitated was filtered, residue washed with diethyl ether (5 times). Combined organic layers were dried, concentrated under reduced pressure giving the desired compound (302 g, 99%) which was used for further reaction.

후처리

  1. customResulting
  2. customreaction mass
  3. customOn completion, solid precipitated
  4. filtrationwas filtered
  5. washresidue washed with diethyl ether (5 times)
  6. customCombined organic layers were dried
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-878164394f97489d80a3f9fe3f7903b7
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09376422B2

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