1H-1,2,4-Triazole-1-propanenitrile, alpha-butyl-alpha-phenyl- → 2-Phenyl-2-[(1,2,4-triazol-1-yl)methyl]-1-hexylamine

HRID 1656013ノート

反応式

HRID 1656013 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH2:7]([C:11]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)([CH2:14][N:15]1[CH:19]=[N:18][CH:17]=[N:16]1)[C:12]#[N:13])[CH2:8][CH2:9][CH3:10]>CCOCC>[C:20]1([C:11]([CH2:14][N:15]2[CH:19]=[N:18][CH:17]=[N:16]2)([CH2:7][CH2:8][CH2:9][CH3:10])[CH2:12][NH2:13])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

参加物

4

反応物 2

HCID 1553371H-1,2,4-Triazole-1-propanenitrile, alpha-butyl-alpha-phenyl-HCID 21226445Aluminium lithium hydride

生成物 1

HCID 199569622-Phenyl-2-[(1,2,4-triazol-1-yl)methyl]-1-hexylamine収率 69.2%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To 21 g (0.55 mole) of lithium aluminum hydride was charged 127 g (0.50 mole) alpha-butyl-alpha-phenyl-1H-1,2,4-triazole-1-propanenitrile in 2500 mL of dry ether over 2.5 hours with stirring under nitrogen. The reaction was stirred for an additional 5 hours after which GLC indicated the reaction was complete. The reaction was quenched with sodium sulfate, filtered and the organic phase separated. The aqueous phase was extracted with 1000 mL of ether. The organics were combined, washed with 3×1.5 liters of ice water, dried, filtered and concentrated without external heating and gave 88 g (69.2% yield) of a pale green oil.

後処理

  1. stirringThe reaction was stirred for an additional 5 hours after which GLC
  2. customThe reaction was quenched with sodium sulfate
  3. filtrationfiltered
  4. customthe organic phase separated
  5. extractionThe aqueous phase was extracted with 1000 mL of ether
  6. washwashed with 3×1.5 liters of ice water
  7. customdried
  8. filtrationfiltered
  9. concentrationconcentrated
  10. temperaturewithout external heating

出典と根拠

ORDレコード
ord-dee0eb136a65420496329f1fa190fb2c
出典データセット
uspto-grants-1993_10
特許番号
US05252594

反応ノート

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