Methanol → Methyl 2-(5-bromopyridin-3-yl)acetate

HRID 391324

반응식

HRID 391324 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]([OH:11])=[O:10])[CH:5]=[N:6][CH:7]=1.S(Cl)(Cl)=O.[CH3:16]O>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]([O:11][CH3:16])=[O:10])[CH:5]=[N:6][CH:7]=1

참가 물질

4

반응 조건

온도
0 °C

실험 절차

To a suspension of 2-(5-bromopyridin-3-yl)acetic acid (5 g, 23.14 mmol) in MeOH (100 mL) was added thionyl chloride (1.858 mL, 25.5 mmol) at 0° C., and the mixture was stirred at 0° C. for 2 h. The mixture was concentrated in vacuo, re-dissolved in DCM (100 mL) and MeOH (10 mL), and saturated NaHCO3 in water (5 mL) was added, followed with NaHCO3 (10 g). To the mixture was added silica gel (10 g) and the mixture was concentrated. The residue was purified by silica chromatography eluting with 0-50% EtOAc-heptane to give methyl 2-(5-bromopyridin-3-yl)acetate. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.64 (s, 3H), 3.80 (s, 2H), 8.01 (dd, J=2.0 Hz, 1H), 8.48 (d, J=1.8 Hz, 1H), 8.61 (d, J=2.3 Hz, 1H).

후처리

  1. concentrationThe mixture was concentrated in vacuo
  2. dissolutionre-dissolved in DCM (100 mL)
  3. additionMeOH (10 mL), and saturated NaHCO3 in water (5 mL) was added
  4. additionTo the mixture was added silica gel (10 g)
  5. concentrationthe mixture was concentrated
  6. customThe residue was purified by silica chromatography
  7. washeluting with 0-50% EtOAc-heptane

출처 및 근거

ORD 기록
ord-7ca55e2e02b34bd78f2b6521da4abef5
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08383827B2

연결된 노트

불러오는 중…