N-carbomethoxy diallyl amine → 2,3-Dihydro-pyrrole-1-carboxylic acid methyl ester

HRID 238965

반응식

HRID 238965 반응식
[C:1]([N:5]([CH2:9][CH:10]=[CH2:11])[CH2:6]C=C)([O:3][CH3:4])=[O:2]>ClCCl.Cl[Ru](=CC1C=CC=CC=1)([P](C1CCCCC1)(C1CCCCC1)C1CCCCC1)([P](C1CCCCC1)(C1CCCCC1)C1CCCCC1)Cl>[CH3:4][O:3][C:1]([N:5]1[CH2:9][CH2:10][CH:11]=[CH:6]1)=[O:2]

참가 물질

4

실험 절차

The obtained N-carbomethoxy diallyl amine (400 g) was dissolved in 1.5 l of dichloromethane purged with nitrogen for 10 minutes by bubbling nitrogen through the stirred solution. In a 5 l flask fitted with a mechanical stirrer and an addition funnel, was charged the Grubb's catalyst (bis(tricyclohexylphosphine)styrylrutheniumdichloride (3 g, 3.9 mmol) under a steady purge. Dichloromethane was added and the resultant dark solution was stirred at r.t. with nitrogen bubbling for 10 minutes. The N-carbomethoxy diallyl amine solution was added to the catalyst solution over a period of 2 hours. When the addition was complete, the solution was stirred at r.t. for 2.5 days. Then, the reaction mixture was concentrated to an oil, which was subsequently purified by vacuum distillation. The desired product was obtained as a clear colorless liquid boiling at about 90° C. (10 mm of Hg) The NMR was consistent with the expected structure.

후처리

  1. custompurged with nitrogen for 10 minutes
  2. customby bubbling nitrogen through the stirred solution
  3. customIn a 5 l flask fitted with a mechanical stirrer and an addition funnel
  4. additionWhen the addition
  5. stirringthe solution was stirred at r.t. for 2.5 days
  6. concentrationThen, the reaction mixture was concentrated to an oil, which
  7. distillationwas subsequently purified by vacuum distillation

출처 및 근거

ORD 기록
ord-eea5c107c1334067a53b6df1007d4b8f
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08642642B2

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