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

HRID 2208771
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HRID 2208771 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

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온도
60 °C

실험 절차

To 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. The resulting reaction mixture was heated at 60° C. for 8 h. On completion, a solid precipitated was filtered, residue washed with diethyl ether (5 times). The combined organic layers were dried, concentrated under reduced pressure giving desired compound (302 g, 99%) which was used as is in subsequent steps.

후처리

  1. additionwere added
  2. customThe resulting reaction mixture
  3. customOn completion, a solid precipitated
  4. filtrationwas filtered
  5. washresidue washed with diethyl ether (5 times)
  6. customThe combined organic layers were dried
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-bb7a596c76d44d59a9b6360212bb2e18
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09376422B2

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