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Hydrochloric Acid → N-(Prop-2-en-1-yl)heptan-1-amine

HRID 232259
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HRID 232259 반응식
[CH2:1]([NH2:4])[CH:2]=[CH2:3].[CH:5](=O)[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].C([BH3-])#N.[Na+].Cl>O.CO>[CH2:1]([NH:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])[CH:2]=[CH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric Acid2회HCID 7853AllylamineHCID 8130HeptanalHCID 5003444Sodium cyanoborohydride

생성물 1

HCID 15629611N-(Prop-2-en-1-yl)heptan-1-amine

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

To 100 mL of methanol is added 2-propenylamine (5.7 g, 0.1 mol), 11.4 g (0.1 mol) of heptaldehyde, and 12 g (0.2 mol) of sodium cyanoborohydride. The pH is adjusted to six with concentrated HCl. Monitor the reaction by thin-layer chromatography. Upon completion, add concentrated HCl until gas evolution ceases. Add 300 mL of H2O and extract once with 200 mL of ether. Add 1N NaOH to the aqueous solution until it is basic and extract twice with 200 mL of ether. Dry the organic phase over Na2SO4. Filter off the drying agent and evaporate the solvent in vacuo to obtain the title compound.

후처리

  1. customMonitor the reaction by thin-layer chromatography
  2. extractionextract once with 200 mL of ether
  3. additionAdd 1N NaOH to the aqueous solution until it
  4. extractionextract twice with 200 mL of ether
  5. dry with materialDry the organic phase over Na2SO4
  6. filtrationFilter off the drying agent
  7. customevaporate the solvent in vacuo

출처 및 근거

ORD 기록
ord-c1e36d85dfd74e0eac0b191df81269ad
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04851526

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