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Iodine → Ethyl 5-benzylnicotinate

HRID 253100
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HRID 253100 반응식
II.[CH2:3](Br)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH2:11]([O:13][C:14](=[O:22])[C:15]1[CH:20]=[C:19](Br)[CH:18]=[N:17][CH:16]=1)[CH3:12].C([O-])(O)=O.[Na+]>CC(N(C)C)=O.C1C=CC=CC=1.CCOC(C)=O.[Zn]>[CH2:11]([O:13][C:14](=[O:22])[C:15]1[CH:20]=[C:19]([CH2:3][C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH:18]=[N:17][CH:16]=1)[CH3:12]
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참가 물질

9

반응물 4

HCID 807IodineHCID 7498Benzyl BromideHCID 140785Ethyl 5-bromopyridine-3-carboxylateHCID 516892Sodium Bicarbonate

생성물 1

HCID 66610002Ethyl 5-benzylnicotinate

시약·촉매·용매 4

HCID 23994Zinc촉매
HCID 241
Benzene
용매
HCID 8857Ethyl Acetate용매
HCID 31374Dimethylacetamide용매

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온도
80 °C

실험 절차

A suspension of Zn (1.0 g, 15 mmol) and I2 (130 mg, 0.5 mmol) in DMA (15 mL) was stirred vigorously until the red color dissipated (3-5 min). Benzyl bromide (1.7 g, 10 mmol) was introduced and the resulting slurry was heated at 80° C. for 2.5 h at which point Cl2Pd(PPh3)2 (250 mg, 0.35 mmol) and a solution of ethyl-5-bromonicotinate (1.1 g, 5.0 mmol) in benzene (10 mL) were introduced and the reaction was heated at 80° C. for 1 h. The reaction was allowed to cool to room temperature and was diluted with EtOAc (100 mL). The mixture was poured into NaHCO3 (5% aqueous, 100 mL). The layers were separated and the aqueous layer was extracted with EtOAc (2×50 mL). The combined organic layers were sequentially washed with H2O (3×100 mL) and brine before being dried over Na2SO4. Concentration and purification by silica gel chromatography (hexane→50% EtOAc/hexane) provided the title compound as a brown oil. MS m/z: 242.1 (M+1).

후처리

  1. custom(3-5 min)
  2. temperatureto cool to room temperature
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted with EtOAc (2×50 mL)
  5. washThe combined organic layers were sequentially washed with H2O (3×100 mL) and brine
  6. dry with materialbefore being dried over Na2SO4
  7. concentrationConcentration and purification by silica gel chromatography (hexane→50% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-50cc732d3b0e420b88462e0f014fffc4
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07872009B2

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