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Hydride → 5-Nitropyridine-2-carbaldehyde

HRID 43074
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HRID 43074 반응식
[H-].C([O:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[CH:9][N:8]=1)=O)C>C(Cl)Cl>[N+:13]([C:10]1[CH:11]=[CH:12][C:7]([CH:5]=[O:4])=[N:8][CH:9]=1)([O-:15])=[O:14]
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참가 물질

4

반응물 2

HCID 166653HydrideHCID 45116302Ethyl 5-nitropicolinate

생성물 1

HCID 151455015-Nitropyridine-2-carbaldehyde수율 49.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
5 °C

실험 절차

Diisobutylaluminiumo hydride (1 M in DCM, 44 mL, 44 mmol, 1.3 equiv) was added dropwise to a cold (−78° C.) solution of 5-nitro-pyridine-2-carboxylic acid ethyl ester (step 39.4) (6.56 g, 33.5 mmol) in DCM (130 mL), under an argon atmosphere. The reaction mixture was allowed to warm to 5° C., quenched by addition of an aqueous solution of potassium sodium tartrate, diluted with DCM and H2O, stirred for 16 h at rt, and filtered through a pad of celite. The filtrate was extracted several times with DCM. The organic phase was washed with H2O and brine, dried (Na2SO4), filtered and concentrated. The residue was purified by by silica gel column chromatography (EtOAc/Hex, 1:1) to provide 2.54 g of the title compound as a beige solid: ESI-MS: 151.1 [M−H]−.

후처리

  1. customquenched by addition of an aqueous solution of potassium sodium tartrate
  2. additiondiluted with DCM and H2O
  3. filtrationfiltered through a pad of celite
  4. extractionThe filtrate was extracted several times with DCM
  5. washThe organic phase was washed with H2O and brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe residue was purified by by silica gel column chromatography (EtOAc/Hex, 1:1)

출처 및 근거

ORD 기록
ord-b1ef0f95d2f54f5da771592b97516bf2
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08536175B2

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