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Methyl iodide → Dimethyl 2-(2-fluoro-4-nitrophenyl)-2-methylmalonate

HRID 1842963
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HRID 1842963 반응식
[F:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH:11]([C:16]([O:18][CH3:19])=[O:17])[C:12]([O:14][CH3:15])=[O:13].[C:20]([O-])([O-])=O.[K+].[K+].CI>CN(C=O)C>[F:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[C:11]([CH3:20])([C:16]([O:18][CH3:19])=[O:17])[C:12]([O:14][CH3:15])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 53429620Dimethyl 2-(2-fluoro-4-nitrophenyl)malonate

생성물 1

HCID 70816610Dimethyl 2-(2-fluoro-4-nitrophenyl)-2-methylmalonate수율 72%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a stirred solution of dimethyl 2-(2-fluoro-4-nitrophenyl)malonate (200 mg, 0.73 mmol, 1.0 eq) and K2CO3 (204 mg 1.47 mmol 2.0 eq) in DMF (5 mL), was added methyl iodide (210 mg, 1.47 mmol 2.0 eq) at RT and the mixture was stirred at RT for 6 h. K2CO3 was filtered out and the filtrate concentrated under vacuum. The residue was diluted with water (50 mL) and extracted with EtOAc (20 mL). The organic layer was separated washed with brine solution, dried over anhydrous Na2SO4 and the solvent evaporated to get dimethyl 2-(2-fluoro-4-nitrophenyl)-2-methylmalonate (150 mg, 71%; TLC system: EtOAc/PE (1:9), Rf: 0.4).

후처리

  1. filtrationK2CO3 was filtered out
  2. concentrationthe filtrate concentrated under vacuum
  3. additionThe residue was diluted with water (50 mL)
  4. extractionextracted with EtOAc (20 mL)
  5. customThe organic layer was separated
  6. washwashed with brine solution
  7. dry with materialdried over anhydrous Na2SO4
  8. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-f4751ed8c1d643cda2eac8ddcf0f13e9
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946204B2

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