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3-(2-Fluorophenyl)propanenitrile → 2-Fluoro-benzenepropanaMine

HRID 2427550
ノート
印刷プレビュー

反応式

HRID 2427550 の反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][C:10]#[N:11]>O1CCCC1>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][CH2:10][NH2:11]
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

3

反応物 1

HCID 390583363-(2-Fluorophenyl)propanenitrile

生成物 1

HCID 226691352-Fluoro-benzenepropanaMine収率 41%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-15 °C

実験手順

A solution of 3-(2-fluorophenyl) propionitrile (9.11 g) in tetrahydrofuran (200 mL) was heated to reflux and treated with borane-methyl sulfide complex (6 mL of ˜10 M, 60 mmol). Approximately half of the volume of the reaction was then distilled off. The mixture was then cooled in a −15° C. bath and treated dropwise with ice water (100 mL). The mixture was then concentrated to a solid. The solid was then dissolved in water (100 mL) and treated with concentrated (12 N)HCl (50 mL). The mixture was heated at reflux for 1 h, cooled to ambient temperature, and equilibrated with diethyl ether (100 mL). The organic solution was removed and the resulting aqueous mixture, cooled by the addition of ice, and then basified (pH>10) by treatment with 10 N NaOH (70 mL). The resulting solution was extracted with diethyl ether (100 mL). The diethyl ether extract was removed, dried over anhydrous MgSO4, filtered and concentrated to afford 3-(2-fluorophenyl)propylamine (3.62 g (41% from 2-fluorobenzaldehyde)). GC/MS gave: m/z (rel.int.) 153 (M+, 10), 136 (100), 109 (50), and 83 (22).

後処理

  1. temperatureto reflux
  2. additiontreated with borane-methyl sulfide complex (6 mL of ˜10 M, 60 mmol)
  3. distillationApproximately half of the volume of the reaction was then distilled off
  4. additiontreated dropwise with ice water (100 mL)
  5. concentrationThe mixture was then concentrated to a solid
  6. dissolutionThe solid was then dissolved in water (100 mL)
  7. additiontreated
  8. concentrationwith concentrated (12 N)HCl (50 mL)
  9. temperatureThe mixture was heated
  10. temperatureat reflux for 1 h
  11. temperaturecooled to ambient temperature
  12. customThe organic solution was removed
  13. temperaturethe resulting aqueous mixture, cooled by the addition of ice
  14. extractionThe resulting solution was extracted with diethyl ether (100 mL)
  15. extractionThe diethyl ether extract
  16. customwas removed
  17. dry with materialdried over anhydrous MgSO4
  18. filtrationfiltered
  19. concentrationconcentrated

出典と根拠

ORDレコード
ord-0fa2ff8e0fab46949a244d8236962e2c
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07968570B2

反応ノート

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