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Phosphorus oxychloride → 5-Bromo-2-chloro-3-ethoxypyridine

HRID 1428522
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HRID 1428522 반응식
[Br:1][C:2]1[CH:3]=[N+:4]([O-])[CH:5]=[C:6]([O:8][CH2:9][CH3:10])[CH:7]=1.O=P(Cl)(Cl)[Cl:14]>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH2:9][CH3:10])[C:5]([Cl:14])=[N:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 53497593Pyridine, 3-bromo-5-ethoxy-, 1-oxide

생성물 1

HCID 713036735-Bromo-2-chloro-3-ethoxypyridine수율 33.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
45 °C

실험 절차

To a solution of 3-bromo-5-ethoxypyridine 1-oxide (40 g, 183 mmol) in DCM (200 mL) at 0° C. was slowly added POCl3 (159 mL, 1701 mmol) over 30 min. Then the resulting solution was warmed to 45° C. for 15 h. The mixture was concentrated and extracted with DCM (2×200 mL), dried over Na2SO4 and concentrated to give 5-bromo-2-chloro-3-ethoxypyridine (30 g, 60.9 mmol, 33.2% yield): 1H NMR (400 MHz, CD3OD) δ 8.00-7.99 (d, J=2.0 Hz, 1H), 7.65-7.64 (d, J=2.0 Hz, 1H), 4.17-4.12 (m, 2H), 1.44 (t, J=7.0 Hz, 2H); ES-LCMS m/z 235 (M+H).

후처리

  1. customat 0° C.
  2. customover 30 min
  3. concentrationThe mixture was concentrated
  4. extractionextracted with DCM (2×200 mL)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-7f06845b88644a11bf4400fc6d61678e
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08937071B2

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