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2-Bromonicotinaldehyde → 1-(2-Bromo-pyridin-3-yl)-4-phenyl-butan-1-ol

HRID 919053
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인쇄 미리보기

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HRID 919053 반응식
[Br:1][C:2]1[C:7]([CH:8]=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[C:10]1([CH2:16][CH2:17][CH2:18][Mg]Br)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>C1COCC1>[Br:1][C:2]1[C:7]([CH:8]([OH:9])[CH2:18][CH2:17][CH2:16][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][CH:5]=[CH:4][N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 47149512-BromonicotinaldehydeHCID 178418471HCID 178418471, 화합물

생성물 1

HCID 866970881-(2-Bromo-pyridin-3-yl)-4-phenyl-butan-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

2-Bromo-pyridine-3-carbaldehyde (1.25 g, 6.72 mmol) was dissolved in THF (10 mL) and cooled to 0° C. 3-phenyl-propyl magnesium bromide (0.5 M in THF, 20.2 mL, 10.08 mmol) was slowly added and the reaction stirred at 0° C. for 1 hour and then at room temperature for 30 minutes. The reaction was monitored by TLC and when complete was quenched with 10 mL of NH4Cl (sat'd, aq.). The volume of THF was reduced and the reaction was submitted to EtOAc/H2O workup. The crude material was purified on silica gel (0-100% EtOAc in hexanes) to give the title compound.

후처리

  1. waitat room temperature for 30 minutes
  2. customcomplete was quenched with 10 mL of NH4Cl (sat'd, aq.)
  3. customThe crude material was purified on silica gel (0-100% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-1c0a5ec6736c4bba97a1ba8ffb48b2a3
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09272990B2

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