참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-carbomethoxy diallyl amine | HCID 4113533 | — |
| 촉매 | HCID 178479819 | HCID 178479819 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2,3-Dihydro-pyrrole-1-carboxylic acid methyl ester | HCID 2751384 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642642B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-eea5c107c1334067a53b6df1007d4b8f |
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| 출처 메모 | uspto-grants-2014_02 |
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