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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129426생성일: 2026년 10월 27일

L-Tartaric acid → D-Tartaric acid

https://huagongshe.com/reaction/129426

반응식

참여 물질

역할이름HCID투입량
반응물L-Tartaric acidHCID 444305—
반응물(4aS-cis-)-6-benzyl-octahydropyrrolo(3.4-b)pyridineHCID 10198297—
반응물[S,S]-8-benzyl-2,8-diazabicyclo[4.3.0]-nonane L-tartrateHCID 10981401—
반응물[R,R]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane L-tartrateHCID 68615090—
용매DimethylformamideHCID 6228—
생성물D-Tartaric acidHCID 439655—
생성물[S,S]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane D-tartrateHCID 22857294—

반응 조건

온도18 °C

반응 단계

73.6 g (0.34 mol) of cis-8-benzyl-2,8-diazabicyclo[4.3.0]nonane dissolved in 111 ml of dimethylformamide is added a drop at a time to a solution of 102.9 g (0.685 mol) of L(+)-tartaric acid in 343 ml of dimethylformamide. The batch is seeded with [R,R]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane L-tartrate and gradually cooled to an interior temperature of 18° C. The crystals are suctioned off and the filtrate seeded with [S,S]-8-benzyl-2,8-diazabicyclo[4.3.0]-nonane L-tartrate and agitated until it crystallizes completely. ([S,S]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane D-tartrate can be obtained from the mother liquor subsequent to concentration and release of the base by purification with D(-)-tartaric acid as described for Method I.) The product is suctioned off, washed with dimethylformamide and isopropyl alcohol, and dried in the air. The crystals are recrystallized from 88% ethanol. 52 g of [S,S]-8-benzyl-2,8-diazabicyclo[4.3-O]nonane L-tartrate trihydrate are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05468742
출처 데이터셋uspto-grants-1995_11
ORD IDord-a8f57c9f8141442fa246a3b1ec4c906e
출처 메모uspto-grants-1995_11