Hydrazine → (6-Cyanohexyl)bis(2-aminoethyl)amine

HRID 1904176

반응식

HRID 1904176 반응식
[C:1]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][N:9]([CH2:23][CH2:24][N:25]1C(=O)C2=CC=CC=C2C1=O)[CH2:10][CH2:11][N:12]1C(=O)C2=CC=CC=C2C1=O)#[N:2].NN>CO>[C:1]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][N:9]([CH2:23][CH2:24][NH2:25])[CH2:10][CH2:11][NH2:12])#[N:2]

참가 물질

4

반응물 2

HCID 9321HydrazineHCID 19811078(6-Cyanohexyl)bis(2-phthalimidoethyl)amine

생성물 1

HCID 19811080(6-Cyanohexyl)bis(2-aminoethyl)amine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of (6-cyanohexyl)bis(2-phthalimidoethyl)amine (13.8g, 0.029 mol) and hydrazine (2.15g, 0.067 mol) in methanol (150 ml) was refluxed for 1.5 hours and allowed to stand overnight. The solvent was removed under reduced pressure and the residue was taken up in water (200 ml) and brought to pH≈2 with HC1. The precipitate was removed by filtration and the filtrate was made basic with solid NaOH. The solution was then concentrated under reduced pressure and extracted with dichloromethane (4×50 ml). The combined organic extracts were dried over Na2SO4 and evaporated under reduced pressure. Kugelrohr distillation of the residue gave pure (6-cyanohexyl)bis(2-aminoethyl)amine as a water white liquid (4.1g-67%) collected between 120° and 140° C. (pot temp) at 0.07 mm Hg. The ir spectrum was consistent with the assigned structure, as was the elemental analysis.

후처리

  1. customThe solvent was removed under reduced pressure
  2. customThe precipitate was removed by filtration
  3. concentrationThe solution was then concentrated under reduced pressure
  4. extractionextracted with dichloromethane (4×50 ml)
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. customevaporated under reduced pressure
  7. distillationKugelrohr distillation of the residue

출처 및 근거

ORD 기록
ord-7ddfd06e3cd44fbd8b5313b8e471bcbe
출처 데이터셋
uspto-grants-1989_06
특허 번호
US04837003

연결된 노트

불러오는 중…