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Water → 5-Bromo-4-methylpicolinaldehyde

HRID 1027593
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HRID 1027593 반응식
C([Mg]Br)(C)C.CN(C)[CH:8]=[O:9].O.[Br:12][C:13]1[C:14]([CH3:20])=[CH:15][C:16](I)=[N:17][CH:18]=1>O1CCCC1>[Br:12][C:13]1[C:14]([CH3:20])=[CH:15][C:16]([CH:8]=[O:9])=[N:17][CH:18]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6228DimethylformamideHCID 263699285-Bromo-2-iodo-4-methylpyridineHCID 178418365HCID 178418365, 화합물

생성물 1

HCID 594745005-Bromo-4-methylpicolinaldehyde

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-15 °C

실험 절차

In an oven-dried flask the compound obtained in Step A (4.67 g) was dissolved in tetrahydrofuran (22 ml). The solution was cooled to −15° C., then isopropyl magnesium bromide (17.2 ml, 15% solution in THF) was added dropwise at a rate to keep the internal temperature between −15° C. to −10° C. The reaction was stirred at this temperature for 1 hour, then anhydrous dimethylformamide (1.8 ml) was added at a rate to keep the internal temperature below 0° C. The reaction was stirred at this temperature for 1 hour, then poured into water and extracted with diethyl ether. The organic layer was dried over sodium sulfate and concentrated in vacuo. The crude title aldehyde product (2.4 g, brown solid) was used as such in the next step.

후처리

  1. custombetween −15° C. to −10° C
  2. customthe internal temperature below 0° C
  3. stirringThe reaction was stirred at this temperature for 1 hour
  4. extractionextracted with diethyl ether
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-4ed6e1dabaa34aa886e05050e644ba6b
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735362B2

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