Chlorotrimethylsilane → 2-Fluoro-4-(trimethylsilyl)aniline

HRID 79003ノート

反応式

HRID 79003 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([F:9])[CH:3]=1.[Li]CCCC.[CH3:15][Si:16](Cl)([CH3:18])[CH3:17]>C1COCC1>[F:9][C:4]1[CH:3]=[C:2]([Si:16]([CH3:18])([CH3:17])[CH3:15])[CH:7]=[CH:6][C:5]=1[NH2:8]

参加物

5

反応物 3

HCID 6397ChlorotrimethylsilaneHCID 1230504-Bromo-2-fluoroanilineHCID 178418339Butyllithium

生成物 1

HCID 595965992-Fluoro-4-(trimethylsilyl)aniline収率 81%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

To a solution of 4-bromo-2-fluoro-phenylamine (114 g, 0.6 mol) in anhydrous THF (750 mL) under inert atmosphere at −78° C. was added a 1.6M solution of nBuLi in hexanes (1500 mL, 2.4 mol) dropwise keeping the internal temperature below −60° C. The reaction mixture was treated dropwise with TMSCl (256 mL, 2.0 mol), keeping the internal temperature below −60° C. The reaction mixture was allowed to warm to 0° C. over a 1 hour period and poured into ice-cold 2M HCl (ca 1 L). The mixture was vigorously stirred for 10 min, then the organic layer was separated, washed with water followed by a saturated solution of potassium carbonate, dried (Na2SO4), filtered and concentrated to give the title compound as a light brown oil (89 g, 81%).

後処理

  1. customthe internal temperature below −60° C
  2. customthe internal temperature below −60° C
  3. customthe organic layer was separated
  4. washwashed with water
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-89f453e2ad9b47f2acf29e973ed771d3
出典データセット
uspto-grants-2014_09
特許番号
US08841462B2

反応ノート

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