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Benzaldehyde → (5-Bromopyridin-2-yl)(phenyl)methanol

HRID 1180436
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HRID 1180436 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][N:3]=1.[Li]CCCC.[CH:14](=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C1(C)C=CC=CC=1>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([CH:14]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[OH:21])=[N:3][CH:4]=1
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참가 물질

5

반응물 3

HCID 240BenzaldehydeHCID 693532,5-DibromopyridineHCID 178418339Butyllithium

생성물 1

HCID 10587663(5-Bromopyridin-2-yl)(phenyl)methanol

시약·촉매·용매 1

HCID 1140Toluene용매2회

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온도
-70 °C

실험 절차

2,5 dibromopyridine (15.0 g, 63.3 mmol) was added to toluene (450 ml) and it was cooled at −70° C. BuLi (1.6 M in hexanes)(41 ml, 66.5 mmol, 1.05 eg) was added dropwise over 1 hour, then reaction mixture was stirred at −70° C. for another hour. Benzaldehyde (7.4 g, 69.6 mmol, 1.1 eg) dissolved in toluene (5 mL) was added slowly. The mixture was stirred at −70° C. for 30 min., then warmed to 0° C. Quenched with Sat NH4Cl (200 mL) and phases partitioned. Aqueous phase was extracted with EtOAc (100 mL) and combined organic washed with brine, dried, evaporated. Residue was chromatographed with 15% EtOAc/hexane to yield the title compound.

후처리

  1. customreaction mixture
  2. additionwas added slowly
  3. stirringThe mixture was stirred at −70° C. for 30 min.
  4. temperaturewarmed to 0° C
  5. customQuenched with Sat NH4Cl (200 mL) and phases
  6. custompartitioned
  7. extractionAqueous phase was extracted with EtOAc (100 mL)
  8. washcombined organic washed with brine
  9. customdried
  10. customevaporated
  11. customResidue was chromatographed with 15% EtOAc/hexane

출처 및 근거

ORD 기록
ord-c6316ac4d11b4c218f6cb04584151146
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07279478B2

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