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Sodium borohydride → Allyl-(1-methyl-pent-4-enyl)-amine

HRID 229791
ノート
印刷プレビュー

反応式

HRID 229791 の反応式
[BH4-].[Na+].[CH2:3]([N:6]=[C:7]([CH3:12])[CH2:8][CH2:9][CH:10]=[CH2:11])[CH:4]=[CH2:5]>CO>[CH2:3]([NH:6][CH:7]([CH3:12])[CH2:8][CH2:9][CH:10]=[CH2:11])[CH:4]=[CH2:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 22036666Allyl-(1-methyl-pent-4-enylidene)-amine

生成物 1

HCID 11788335Allyl-(1-methyl-pent-4-enyl)-amine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Sodium borohydride (2.7 g, 71 mmol) was added portionwise to a stirred solution of allyl-(1-methyl-pent-4-enylidene)-amine (6.5 g, 47 mmol) in MeOH (100 ml) at 0 C. The reaction mixture was stirred for 30 minutes, then warmed to RT. Approximately 90 ml of MeOH was removed from the reaction mixture by rotary evaporation, then the reaction mixture was diluted with ether (200 ml), then extracted with water then brine. The combined organics were dried with MgSO4, filtered, concentrated in vacuo by rotary evaporation to give a pale yellow liquid that was used in the next reaction without further purification (5.2 g, 80%).

後処理

  1. customApproximately 90 ml of MeOH was removed from the reaction mixture by rotary evaporation
  2. additionthe reaction mixture was diluted with ether (200 ml)
  3. extractionextracted with water
  4. dry with materialThe combined organics were dried with MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo by rotary evaporation
  7. customto give a pale yellow liquid that
  8. customwas used in the next reaction without further purification (5.2 g, 80%)

出典と根拠

ORDレコード
ord-907e6e04de304fa596e50c1e755580f1
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07563784B2

反応ノート

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