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Ethylenediamine → Benzyl N-(2-aminoethyl)carbamate

HRID 85355
ノート
印刷プレビュー

反応式

HRID 85355 の反応式
[CH2:1]([NH2:4])[CH2:2][NH2:3].CC1C(Br)=C(O)C(Br)=CC=1C1(C2C=C(Br)C(O)=C(Br)C=2C)OS(=O)(=O)C2C=CC=CC1=2.CS(O)(=O)=O.[CH:41]1[CH:46]=[CH:45][C:44]([CH2:47][O:48][C:49](Cl)=[O:50])=[CH:43][CH:42]=1.C(O[K])(C)=O>O.C(O)C.C(COC)OC>[NH2:3][CH2:2][CH2:1][NH:4][C:49](=[O:50])[O:48][CH2:47][C:44]1[CH:45]=[CH:46][CH:41]=[CH:42][CH:43]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 5

HCID 3301EthylenediamineHCID 6395Methanesulfonic AcidHCID 6451Bromocresol GreenHCID 10387Benzyl chloroformateHCID 178476685HCID 178476685、化合物

生成物 1

HCID 2794257Benzyl N-(2-aminoethyl)carbamate収率 51%

試薬・触媒・溶媒 3

HCID 702
Ethanol
溶媒
HCID 962Water溶媒2 回
HCID 80711,2-Dimethoxyethane溶媒

実験手順

Ethylenediamine (1.0 g, 16.7 mmol) is dissolved in water (3.0 mL) containing bromocresol green as an indicator. Methane sulfonic acid (2.8 g, 31 mmol) in water (3.0 mL) is added until a blue to pale yellow color transition is just achieved. The solution is diluted with ethanol (8.0 mL) and vigorously stirred. To the mixture was added the solution of Cbz-Cl (2.8 g, 16.7 mmol) in dimethoxyethane (4 mL) and 50% w/v aqueous AcOK (10 mL) at 20° C. simultaneously to maintain the pale yellow-green color of the indicator. After the additions are complete the mixture was stirred (RT, 1 h) and concentrated at low temperature under vacuum to removed the volatiles. The residue was shaken with water (20 mL) and filtered. The filtrate was then washed with toluene (3×50 mL), basified with excess 40% aqueous NaOH and extracted with toluene (3×50 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4 and evaporated to give benzyl 2-aminoethylcarbamate as an oil (1.65 g, 51%). Mass calculated for C10H14N2O2=194.23; found: [M−H]+=193.3.

後処理

  1. customat 20° C.
  2. temperatureto maintain the pale yellow-green color of the indicator
  3. stirringwas stirred (RT, 1 h)
  4. concentrationconcentrated at low temperature under vacuum
  5. customto removed the volatiles
  6. stirringThe residue was shaken with water (20 mL)
  7. filtrationfiltered
  8. washThe filtrate was then washed with toluene (3×50 mL)
  9. extractionextracted with toluene (3×50 mL)
  10. washThe organic layer was washed with brine (50 mL)
  11. dry with materialdried over Na2SO4
  12. customevaporated

出典と根拠

ORDレコード
ord-4a860e4ef292473a9a0e191aba6087bb
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08846972B2

反応ノート

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