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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1584585생성일: 2026년 10월 26일

1-(2,3-dihydro-1H-isoindol-2-yl)ethan-1-one → trans-hexahydro-N-acetylisoindoline

https://huagongshe.com/reaction/1584585

반응식

참여 물질

역할이름HCID투입량
반응물1-(2,3-dihydro-1H-isoindol-2-yl)ethan-1-oneHCID 15444356—
반응물cis-hexahydro-N-acetylisoindolineHCID 54454143—
반응물HCID 178418361HCID 178418361—
촉매HCID 178503044HCID 178503044—
용매MethanolHCID 887—
생성물trans-hexahydro-N-acetylisoindolineHCID 867543700.2%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05932744
출처 데이터셋uspto-grants-1999_08
ORD IDord-47db33fc981c43b0bae87edf744595c0
출처 메모uspto-grants-1999_08