A method for resolution and preparation of optically pure r-2-naphthylethylamine

Abstract

The invention relates to a method for preparing R-2-naphthylethylamine by dynamic kinetic resolution. Using 2‑naphthylethylamine as raw material, Novozym 435 as resolution catalyst, D‑(‑)‑O‑acetylmandelic acid as acyl donor, KT‑02 (nickel catalyst) as racemization catalyst, in autoclave 2-Naphthylethylamine is completely converted to obtain (R)-(1-(2-naphthyl)ethyl)acetamide (ee value 99%); acidolysis is carried out after amide purification to obtain R-2 ‑Naphthylethylamine salt, the salt is then basified, extracted, dried, concentrated, etc. to obtain R‑2‑naphthylethylamine. The product yield of each step can reach more than 90%, and the ee value is greater than 99%. The invention has the characteristics of cheap and easy to obtain racemic catalyst, complete utilization of raw materials, good product yield, high optical purity and the like. In the production and preparation of R-2-naphthylethylamine, it has great guidance and application value.

Description

technical field [0001] The invention relates to a resolution and preparation method of optically pure chiral amine, in particular to a resolution and preparation method of optically pure R-2-naphthylethylamine. Background technique [0002] Optically pure chiral amines are very important pharmaceutical intermediates. At present, optically pure chiral amines are mainly obtained through the following methods: enzymatic resolution (Indian J. Chem. Sect. B 2005, 44, 1312-1316; J. Org. Chem. 1997, 62, 3488-3495); Chemical resolution: resolution with chiral α-hydroxyphenylacetic acid (US6342636; Tetrahedron: asymmetry, 1998, 9, 2219-2212) or protected chiral glycerol derivatives (Tetrahedron: asymmetry, 1996, 7, 1117-1122 ; Tetrahedron: asymmetry, 2002, 13, 2277-2282); obtained by asymmetric synthesis of the corresponding aldehyde (WO2004 / 110976; J. Org. Chem. 1992, 57, 1237-1241). [0003] Among the existing methods, the cost of asymmetric synthesis is high and it is often diff...

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Problems solved by technology

[0003] Among the existing methods, asymmetric synthesis is costly and often difficult to obtain products with high optical purity; chemical resolution and enzymatic kinetic resolution have the disadvantage of low raw material utilization, which is only 50% at most; In the reported enzymatic dynamic kinetic resolution method, the racemization catalysts used are usually complexes of some noble metals such as ruthenium and rhodium. These racemization catalysts are extremely expensive, and when these racemization catalysts are used in the resolution preparation process , although a high conversion rate is achieved, it is difficult to obtain a high optical purity of the product

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