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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1089657생성일: 2026년 10월 25일

DL-Ephedrine → Pseudoephedrine

https://huagongshe.com/reaction/1089657

반응식

참여 물질

역할이름HCID투입량
반응물DL-EphedrineHCID 5032—
반응물MethylamineHCID 6329—
반응물EphedrineHCID 9294—
생성물PseudoephedrineHCID 7028—

반응 단계

The combination of yeast transformation of benzaldehyde to produce PAC and chemical conversion of the PAC to make 1-ephedrine is described in U.S. Pat. No. 1,956,950. The PAC can be converted by a chemical reductive amination with methylamine to optically pure L-ephedrine as follows: ##STR2## The 1-ephedrine can then converted in high yield to d-pseudoephedrine as follows: ##STR3## It is apparent from this reaction scheme that microbial transformation of benzaldehyde by yeast to form L-(-)phenyl acetyl carbinol in high yield and purity is of prime importance for successful commercial operation of the synthetic route.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05079145
출처 데이터셋uspto-grants-1992_01
ORD IDord-c9ee2c214413439988f36bc372be76e0
출처 메모uspto-grants-1992_01