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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583007생성일: 2026년 10월 27일

Hexadecane → N-(2-Phenylacetyl)-4-Keto-D,L-Proline Methyl Ester

https://huagongshe.com/reaction/583007

반응식

참여 물질

역할이름HCID투입량
반응물HexadecaneHCID 11006—
반응물N-(2-phenylacetyl)-4-keto-D-proline methyl esterHCID 53997628—
반응물N-(2-phenylacetyl)-4-keto-L-proline methyl esterHCID 53997629—
용매DichloromethaneHCID 6344—
용매Sodium AcetateHCID 517045—
생성물N-(2-Phenylacetyl)-4-Keto-D,L-Proline Methyl EsterHCID 21226264—

반응 단계

An aqueous solution (1.0 mL) containing 19 mM of N-(2-phenylacetyl)-4-keto-D-proline methyl ester and 19 mM of N-(2-phenylacetyl)-4-keto-L-proline methyl ester in 0.200M sodium acetate (pH 5.0) and 25 mg/mL of Candida antartica lipase fraction B was mixed at 25° C. The reaction mixture was analyzed by mixing with an equivalent volume of 20 mM hexadecane in dichloromethane for 3 minutes, which resulted in the complete extraction of the unreacted D- and L-isomers. The dichloromethane extract was then analyzed by chiral gas chromatography on a Chiraldex G-TA column (Advanced Separation Technologies, Inc., 50 m×0.32 mm ID) to determine the relative amounts of the unreacted D- and L-isomers. After 28 h, 97% of the D-isomer and 28% of the L-isomer remained, yielding a 55% enantiomeric excess of the D-isomer at 38% conversion of the racemic mixture (E=28).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05928933
출처 데이터셋uspto-grants-1999_07
ORD IDord-5495bc3290b2416f89e7039bb9585889
출처 메모uspto-grants-1999_07