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Bromine → 3-Bromo-5-chloro-2-methoxypyridine

HRID 280187
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HRID 280187 반응식
C([O-])(=O)C.[Na+].[Cl:6][C:7]1[CH:8]=[CH:9][C:10]([O:13][CH3:14])=[N:11][CH:12]=1.[Br:15]Br>C(O)(=O)C>[Br:15][C:9]1[C:10]([O:13][CH3:14])=[N:11][CH:12]=[C:7]([Cl:6])[CH:8]=1
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참가 물질

5

반응물 3

HCID 24408BromineHCID 517045Sodium AcetateHCID 47382765-Chloro-2-methoxypyridine

생성물 1

HCID 135677513-Bromo-5-chloro-2-methoxypyridine

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

반응 조건

온도
80 °C

실험 절차

To a stirred suspension of 2.5 g of anhydrous sodium acetate in 10 ml of acetic acid was added 4.3 g of 5-chloro-2-methoxypyridine followed by a solution of 3.1 ml of bromine in 10 ml of acetic acid. The mixture was warmed to 80° C. for 6 hours and then allowed to cool and stirred at 23° C. for 64 hours. It was then partitioned between ether and water and the resulting ether layer was washed with aqueous 1N sodium hydroxide solution and then with aqueous 5% sodium bisulfite solution, dried over potassium carbonate and concentrated at reduced pressure to leave a residual brown solid. This residue was bulb-to-bulb distilled with the material distilling at 140°-150° C. at 20 torr collected to give 3-bromo-5-chloro-2-methoxypyridine as a solid melting at about 45°-47.5° C.

후처리

  1. temperatureto cool
  2. customIt was then partitioned between ether and water
  3. washthe resulting ether layer was washed with aqueous 1N sodium hydroxide solution
  4. dry with materialwith aqueous 5% sodium bisulfite solution, dried over potassium carbonate
  5. concentrationconcentrated at reduced pressure
  6. customto leave a residual brown solid
  7. distillationdistilled with the material
  8. distillationdistilling at 140°-150° C. at 20 torr
  9. customcollected

출처 및 근거

ORD 기록
ord-a57e399a64054ad68499af284a975daa
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04588733

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