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HRID 1584579作成日:2026年10月26日

Hydrochloric Acid → (2-Methylcyclohexyl)methanamine

https://huagongshe.com/reaction/1584579

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物IsoindolineHCID 422478—
反応物cis-OctahydroisoindoleHCID 10964494—
反応物HCID 178418361HCID 178418361—
触媒HCID 178503044HCID 178503044—
生成物(2-Methylcyclohexyl)methanamineHCID 212250480.4%
生成物(3aR,7aR)-Octahydro-1H-isoindoleHCID 366891950.3%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05932744
出典データセットuspto-grants-1999_08
ORD IDord-55e265499b7a48db91d5f4bebec609f5
出典メモuspto-grants-1999_08