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

HRID 229791
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HRID 229791 반응식
[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]
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참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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%).

후처리

  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%)

출처 및 근거

ORD 기록
ord-907e6e04de304fa596e50c1e755580f1
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07563784B2

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