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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452008생성일: 2026년 10월 23일

D-Proline → dibenzyl 1-((2S)-1-hydroxy-3-(tetrahydro-2H-pyran-3-yl)propan-2-yl)hydrazine-1,2-dicarboxylate

https://huagongshe.com/ko/reaction/452008

반응식

참여 물질

역할이름HCID투입량
반응물D-ProlineHCID 8988—
반응물1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylateHCID 75557—
반응물Sodium borohydrideHCID 4311764—
반응물Tetrahydro-2H-pyran-3-propanalHCID 15676001—
용매EthanolHCID 702—
용매AcetonitrileHCID 6342—
생성물dibenzyl 1-((2S)-1-hydroxy-3-(tetrahydro-2H-pyran-3-yl)propan-2-yl)hydrazine-1,2-dicarboxylateHCID 5801741381%

반응 조건

온도0 °C

반응 단계

To a stirred solution of 3-(tetrahydro-2H-pyran-3-yl)propanal (8.25 g, 0.058 mol) and dibenzyl azodicarboxylate (94%, 12.3 g, 0.041 mol) in MeCN (250 mL) at 0° C. was added (R-proline) (0.47 g, 0.0041 mol). After stirring the mixture at 0° C. for 15 hr. ethanol (100 mL) and NaBH4 (1.56 g, 0.041 mol) was added, and the mixture was stirred at 0° C. for 40 min. The reaction was quenched by slow addition of 10% aqueous citric acid (15 ml), and the whole solution was concentrated in vacuo. This residue was diluted with EtOAc (200 ml), washed with saturated brine (1×50 mL), dried over Na2SO4, and concentrated in vacuo to give the crude product, which was purified through column chromatography to give dibenzyl 1-((2S)-1-hydroxy-3-(tetrahydro-2H-pyran-3-yl)propan-2-yl)hydrazine-1,2-dicarboxylate (14.68 g, 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08487108B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-05708893fea3414699cd85f2ea037a9c
출처 메모uspto-grants-2013_07