ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Isoamyl Nitrite → 2-Fluoro-3-methyl-1,1'-biphenyl

HRID 1065578
ノート
印刷プレビュー

反応式

HRID 1065578 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:3]=1N.[F:15][B-](F)(F)F.[H+].N(OCCC(C)C)=O>O1CCCC1.O>[F:15][C:3]1[C:2]([CH3:1])=[CH:7][CH:6]=[CH:5][C:4]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1
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 3

HCID 8053Isoamyl NitriteHCID 28118Tetrafluoroboric acidHCID 6030843-Methyl-[1,1'-biphenyl]-2-amine

生成物 1

HCID 202706122-Fluoro-3-methyl-1,1'-biphenyl

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

A stirred solution of 3-methyl-[1,1'-biphenyl]-2-amine (7.5 g, 0.041 mole, as prepared in method K) in 20 ml of tetrahydrofuran was cooled to 5°. A solution of 40 ml tetrafluoroboric acid (48-50% solution) in 20 ml of water was added to the cooled reaction mixture, followed by dropwise addition of isoamyl nitrite (6.2 g, 0.053 mole). After complete addition, the reaction mixture was stirred for 15 minutes and filtered. The filter cake was rinsed successively with 50 ml each of 5% aqueous tetrafluoroboric acid, cold methanol, and cold diethyl ether. The filter cake was added to 100 ml of toluene and the mixture stirred and heated at 60° until the solid dissolved and bubbling subsided. The mixture was heated at reflux for 30 minutes, then held at room temperature for two days, causing separation of an oil. The toluene was decanted from the oil and evaporated under reduced pressure to give a second oil, which was purified by column chromatography on silica gel, elution by toluene:n-heptane (6:94), to give 2-fluoro-3-methyl-[1,1'-biphenyl].

後処理

  1. additionAfter complete addition
  2. filtrationfiltered
  3. washThe filter cake was rinsed successively with 50 ml each of 5% aqueous tetrafluoroboric acid, cold methanol, and cold diethyl ether
  4. additionThe filter cake was added to 100 ml of toluene
  5. stirringthe mixture stirred
  6. temperatureheated at 60° until the solid
  7. dissolutiondissolved
  8. custombubbling
  9. temperatureThe mixture was heated
  10. temperatureat reflux for 30 minutes
  11. waitheld at room temperature for two days
  12. customseparation of an oil
  13. customThe toluene was decanted from the oil
  14. customevaporated under reduced pressure
  15. customto give a second oil, which
  16. customwas purified by column chromatography on silica gel, elution by toluene:n-heptane (6:94)

出典と根拠

ORDレコード
ord-c0d1c345fc734cca9bc502ca14d723d7
出典データセット
uspto-grants-1982_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04329518

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート