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HRID 1077095作成日:2026年10月27日

4,4-Diaminodiphenylmethane → 4,4'-Diaminodicyclohexylmethane

https://huagongshe.com/reaction/1077095

反応式

関与物質

役割名称HCID仕込み量
反応物4,4-DiaminodiphenylmethaneHCID 7577—
触媒RutheniumHCID 23950—
生成物4,4'-DiaminodicyclohexylmethaneHCID 15660—

反応手順

Due to these disadvantages and others, the utilization of catalysts containing metallic ruthenium has become preferred in the art in such hydrogenation processes as described in U.S. Pat. Nos. 2,606,924; 2,606,925; 2,494,563; 3,347,917; 3,676,495; and others. U.S. Pat. No. 2,606,924 to Whitman (1952) and U.S. Pat. No. 2,494,563 to Kirk, et al. (1950) describe processes for the preparation of certain stereoisomeric bis (4-aminocyclohexyl)methanes by the hydrogenation of bis(4-aminophenyl)methane with a ruthenium metal catalyst in the presence or absence of volatile organic solvent. More particularly, Whitman (2,606,924) discloses that steroisomeric bis(4-aminocyclohexyl)methane mixtures liquid at normal temperatures can be produced by the hydrogenation of bis(4-aminophenyl)methane at a temperature of 75°-125°C. and a pressure of between 100-15,000 psi in the presence of a ruthenium catalyst. Kirk, et al. (2,494,563) teach that the hydrogenation of bis(4-aminophenyl)methane in the presence of a ruthenium catalyst at temperatures between 140°-250°C. and pressures above 500 psi, e.g., 1,500-3,500 psi, results in a reaction product which, upon distillation and redistillation in vacuo, provides stereoisomeric bis (4-aminocyclohexyl)methane mixtures having a freezing point above 40°C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03959374
出典データセットuspto-grants-1976_05
ORD IDord-83e6e052ff6c4b37ad59ddf27dcc96dd
出典メモuspto-grants-1976_05