참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexadecane | HCID 11006 | — |
| 반응물 | N-(methoxycarbonyl)-4-keto-L-proline methyl ester | HCID 53913858 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Sodium Acetate | HCID 517045 | — |
| 생성물 | N-(methoxycarbonyl)-4-keto-D-proline methyl ester | HCID 11275680 | — |
반응 단계
An aqueous solution (5.0 mL) containing 25 mM N-(methoxycarbonyl)-4-keto-Dproline methyl ester and 25 mM N-(methoxycarbonyl)-4-keto-L-proline methyl ester in 0.200M sodium acetate (pH 5.0) was mixed with 2.5 g of immobilized Candida antartica lipase fraction B (Boehringer Mannheim, CHIRAZYME® L-2, c.-f., C2, lyo.) at 25° C. The reaction mixture was analyzed after 31 h by mixing the entire reaction mixture with 5.0 mL of 20 mM hexadecane in dichloromethane for 10 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 amounts of the unreacted D- and L-isomers. After 31 h, an 85% enantiomeric excess of N-(methoxycarbonyl)-4-keto-D-proline methyl ester was obtained at 41% conversion of the racemic mixture.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05928933 |
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| 출처 데이터셋 | uspto-grants-1999_07 |
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| ORD ID | ord-b4e20b41f8c94ccfb563ade87bed2390 |
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| 출처 메모 | uspto-grants-1999_07 |
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