Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-(2,3-dihydro-1H-isoindol-2-yl)ethan-1-one → trans-hexahydro-N-acetylisoindoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-(2,3-dihydro-1H-isoindol-2-yl)ethan-1-one | HCID 15444356 | — |
| 반응물 | cis-hexahydro-N-acetylisoindoline | HCID 54454143 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | HCID 178503044 | HCID 178503044 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | trans-hexahydro-N-acetylisoindoline | HCID 86754370 | 0.2% |
반응 단계
In a 3-liter GL autoclave fitted with a electromagnetic stirrer are added 175 g of N-acetylisoindoline, 825 g of methylalcohol and 17 g of 5% ruthenium-carbon catalyst (50% water-containing). The reaction mixture is subjected to a hydrogen-pressure of 20 kg/cm2 and a temperature of 110° C. After a 8 hour hydrogen introduction, the drop in the rate of the hydrogen-absorption is observed, at this point the introduction of hydrogen is ceased to terminate the reaction. After the termination of reaction, the catalyst is filtered out from the reacted solution. By the result of the capillary chromatographic analysis, the yield of cis-hexahydro-N-acetylisoindoline is 93.7%. In addition, 0.2% of trans-hexahydro-N-acetylisoindoline is formed.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05932744 |
| 출처 데이터셋 | uspto-grants-1999_08 |
| ORD ID | ord-47db33fc981c43b0bae87edf744595c0 |
| 출처 메모 | uspto-grants-1999_08 |