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HRID 723302作成日:2026年10月26日

Octane → (R)-(+)-1-Benzyl-3-pyrrolidinol

https://huagongshe.com/reaction/723302

反応式

関与物質

役割名称HCID仕込み量
反応物OctaneHCID 356—
反応物DecaneHCID 15600—
反応物N-benzyl-3-pyrrolidinolHCID 69889—
反応物1-(Phenylmethyl)pyrrolidineHCID 122501—
溶媒HexaneHCID 8058—
生成物(R)-(+)-1-Benzyl-3-pyrrolidinolHCID 643472—

反応手順

It has been found that alkane-degrading microorganisms are excellent biocatalysts for the hydroxylation of N-benzylpyrrolidine to optically active N-benzyl-3-hydroxy-pyrrolidine. Examples are bacteria degrading n-alkane containing 4 or more C-atoms. By screening with a microtiter plate, 25 of a set of 70 strains degrading n-hexane, n-octane, n-decane, or n-dodedane, were found to be able to catalyse this hydroxylation (example 5). The enantioselectivity and relative activity of 14 selected alkane-degrading strains are shown in table 3 (example 6). Hydroxylation of N-benzylpyrrolidine with Pseudomonas putida P1 gave (R)-N-benzyl-3-hydroxypyrrolidine in 62% e.e.; hydroxylation of N-benzylpyrrolidine with the isolate HXN-1100 gave (R)-N-benzyl-3-hydroxypyrrolidine in 70% e.e.; surprisingly, hydroxylation of N-benzylpyrrolidine with the isolate HXN-200 gave (S)-N-benzyl-3-hydroxypyrrolidine in 53% e.e. (Pseudomonas putida P1 was isolated with n-octane as carbon source by van Beilen, J., ETH Zurich; the isolates HXN-1100 and HXN-200 were isolated with n-hexane as carbon source by Engesser, K.-H. and Plaggemeier, Th., University of Stuttgart; all these strains are in the strain collection of institute of Biotechnology, ETH Zurich).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07141412B2
出典データセットuspto-grants-2006_11
ORD IDord-3e391f8587f04aff8b663f6c6a4448ce
出典メモuspto-grants-2006_11