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Heptane → Tert-butyl 5-bromo-2,4-difluoronicotinate

HRID 1481770
ノート
印刷プレビュー

反応式

HRID 1481770 の反応式
[F:1][C:2]1[N:14]=[CH:13][CH:12]=[C:11]([F:15])[C:3]=1[C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5].[Li+].CC([N-]C(C)C)C.CCCCCCC.[Br:31]C(Br)(Cl)C(Cl)(Cl)Cl>C1COCC1>[Br:31][C:12]1[CH:13]=[N:14][C:2]([F:1])=[C:3]([C:11]=1[F:15])[C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8900HeptaneHCID 2724682Lithium diisopropylamideHCID 137826771,1-Dibromo-1,2,2,2-tetrachloroethaneHCID 71281946Tert-butyl 2,4-difluoronicotinate

生成物 1

HCID 71281815Tert-butyl 5-bromo-2,4-difluoronicotinate収率 42.5%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒
2 回

実験手順

Into a solution of tert-butyl 2,4-difluoronicotinate (0.95 g, 4.4 mmol) in THF (15 mL) at −78° C. was added a solution of LDA in heptane (1.5 M×3.5 mL, 5.3 mmol) dropwise. The mixture was stirred for 10 min. Then a solution of dibromotetrachloroethane (1.86 g, 5.7 mmol) in THF (4.0 mL) was added dropwise. After 15 min, the temperature was allowed to rise to room temperature slowly. The reaction was quenched with saturated NH4Cl. The mixture was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated to give a residue, which was purified by silica chromatography (5-50% dichloromethane in hexanes) to give tert-butyl 5-bromo-2,4-difluoronicotinate (0.55 g, 42%).

後処理

  1. waitAfter 15 min
  2. customto rise to room temperature
  3. customThe reaction was quenched with saturated NH4Cl
  4. extractionThe mixture was extracted with ethyl acetate
  5. dry with materialThe combined organic layers were dried over sodium sulfate
  6. customevaporated
  7. customto give a residue, which
  8. customwas purified by silica chromatography (5-50% dichloromethane in hexanes)

出典と根拠

ORDレコード
ord-40f1cead9577488ea2d7dca0e6ee552e
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409905B2

反応ノート

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