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Ammonia → HCID 131717149, 화합물

HRID 1090481
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HRID 1090481 반응식
N.[H][H].COC(C)C#N.[C:10]([CH2:12][CH2:13][O:14][CH:15]([O:17][CH2:18][CH2:19][C:20]#[N:21])[CH3:16])#[N:11]>[Ni].CO>[NH2:21][CH2:20][CH2:19][CH2:18][O:17][CH:15]([O:14][CH2:13][CH2:12][CH2:10][NH2:11])[CH3:16].[CH3:15][O:14][CH2:13][CH2:12][CH2:10][NH2:11]
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참가 물질

7

반응물 4

HCID 222AmmoniaHCID 1418292-MethoxypropanenitrileHCID 13931490HCID 13931490, 화합물HCID 178418361HCID 178418361, 화합물3회

생성물 1

HCID 131717149HCID 131717149, 화합물

시약·촉매·용매 2

HCID 935Nickel촉매
HCID 887
Methanol
용매

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온도
90 °C

실험 절차

Into a 2 liter stirred autoclave was placed 60 g of Raney nickel 2400 and 120 g of anhydrous ammonia. A heel of 200 g of methanol was then pumped into the reactor and the reactor externally heated to 90° C. The pressure was raised to 850 psig with hydrogen. The crude product mixture of methoxypropionitrile (MOPN) and bis(cyanoethoxy)ethane from Example 4 was then pumped into the autoclave at a rate of 5.0 g/min until 999 g of the mixture had been admitted. During the addition the temperature was maintained at 90° C. and the pressure at 850 psig with hydrogen. Following the addition, hydrogen uptake ceased within 30 min. and the reaction was terminated. The contents of the autoclave were cooled and then filtered through Celite™ filtration aid. The filtrate was analyzed by GC and found to be comprised of 16.8 wt % 3-methoxypropylamine (MOPA), 77.0 wt % of bis(3-aminopropoxy)ethane, 0.89 wt % of 3-aminopropoxyethanol, 1.96 wt % of N-methoxypropyl-bis(3-amino-propoxy)ethane, 0.35 wt % of bis(3-methoxypropyl)amine and 3.0 wt % of bis(aminopropoxyethoxypropyl)amine.

후처리

  1. additionDuring the addition the temperature
  2. temperaturewas maintained at 90° C.
  3. customthe reaction was terminated
  4. temperatureThe contents of the autoclave were cooled
  5. filtrationfiltered through Celite™ filtration aid

출처 및 근거

ORD 기록
ord-cfaf44a29a2c489ab2d1cf36ef4eaa28
출처 데이터셋
uspto-grants-1992_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05081305

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