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Formaldehyde → (6-Bromo-2-fluoropyridin-3-YL)methanol

HRID 57917
ノート
印刷プレビュー

反応式

HRID 57917 の反応式
C(NC(C)C)(C)C.[Li+].CCC[CH2-].CCCCCC.[Br:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([F:26])[N:21]=1.[CH2:27]=[O:28]>C1COCC1>[Br:19][C:20]1[N:21]=[C:22]([F:26])[C:23]([CH2:27][OH:28])=[CH:24][CH:25]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 712FormaldehydeHCID 7912DiisopropylamineHCID 8058HexaneHCID 61028n-Butyl lithiumHCID 6394382-Bromo-6-fluoropyridine

生成物 1

HCID 71303921(6-Bromo-2-fluoropyridin-3-YL)methanol収率 36.1%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒
2 回

反応条件

温度
0 °C

実験手順

To Diisopropylamine (22.001 mmol; 2240 mg; 3.13 mL) in THF (40 mL) at 0° C. was added N-Butyllithium (2.5 mol/L) in Hexane (24.001 mmol; 9.6 mL). The reaction was stirred at 0° C. for 0.5 h, and then cooled to −78° C. 2-bromo-6-fluoro-pyridine (20.001 mmol; 3520.0 mg) in THF (10 mL) was added dropwise. The mixture was stirred at −78° C. for 2.5 h. Paraformaldehyde (40.002 mmol; 3603.3 mg) was added rapidly. The mixture was allowed to warm to room temperature and stirred overnight. The reaction was quenched with water. The layers were separated. The aqueous layer was extracted with EtOAc. The combined organic layers were concentrated and the residue was purified on silica eluted with 0 to 50% EtOAc in Heptane to afford (6-bromo-2-fluoro-3-pyridyl)methanol (1.4888 g, 36%).

後処理

  1. temperaturecooled to −78° C
  2. stirringThe mixture was stirred at −78° C. for 2.5 h
  3. temperatureto warm to room temperature
  4. stirringstirred overnight
  5. customThe reaction was quenched with water
  6. customThe layers were separated
  7. extractionThe aqueous layer was extracted with EtOAc
  8. concentrationThe combined organic layers were concentrated
  9. customthe residue was purified on silica
  10. washeluted with 0 to 50% EtOAc in Heptane

出典と根拠

ORDレコード
ord-4978cefcf13e4e80a5ca5025f4f3b682
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09434725B2

反応ノート

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