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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 723302생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/723302

반응식

참여 물질

역할이름HCID투입량
반응물OctaneHCID 356—
반응물DecaneHCID 15600—
반응물N-benzyl-3-pyrrolidinolHCID 69889—
반응물1-(Phenylmethyl)pyrrolidineHCID 122501—
용매HexaneHCID 8058—
생성물(R)-(+)-1-Benzyl-3-pyrrolidinolHCID 643472—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141412B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-3e391f8587f04aff8b663f6c6a4448ce
출처 메모uspto-grants-2006_11