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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1584579생성일: 2026년 10월 26일

Hydrochloric Acid → (2-Methylcyclohexyl)methanamine

https://huagongshe.com/reaction/1584579

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IsoindolineHCID 422478—
반응물cis-OctahydroisoindoleHCID 10964494—
반응물HCID 178418361HCID 178418361—
촉매HCID 178503044HCID 178503044—
생성물(2-Methylcyclohexyl)methanamineHCID 212250480.4%
생성물(3aR,7aR)-Octahydro-1H-isoindoleHCID 366891950.3%

반응 단계

In a 3-liter GL (Glass Lining) autoclave fitted with a electromagnetic stirrer are added 129 g of isoindoline, 545 g of 7.2% hydrochloric acid aqueous solution (pH 4.0) and 26 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 130° C. After a 2 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-hexahydroisoindoline is 98.3%. In addition, 0.3% of trans-hexahydroisoindoline and 0.4% of 2-methylcyclohexylmethylamine is formed. After cooling the reacted solution, 240 g of 20% sodium hydroxide aqueous solution is added to neutralize, and it is extracted with toluene. After concentrating the organic phase, the residue is purified by distillation to give 128.0 g of cis-hexahydroisoindoline (yield 94.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05932744
출처 데이터셋uspto-grants-1999_08
ORD IDord-55e265499b7a48db91d5f4bebec609f5
출처 메모uspto-grants-1999_08