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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 431753생성일: 2026년 10월 26일

Imidazole → cis4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-proline

https://huagongshe.com/reaction/431753

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물(2R,4R)-1-((benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688416—
용매DimethylformamideHCID 6228—
용매Ethyl acetate hexaneHCID 21226206—
생성물cis4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-prolineHCID 6999564189.5%

반응 단계

To a mixture of cis4-hydroxy-N-benzyloxycarbonyl-D-proline (18.74 g) and imidazole (11.56 g) in DMF (100 mL) was added TBDMSCl (23.36 g) at 5° C. After stirring at room temperature for 16 hours, the reaction mixture was diluted with EtOAc-hexane (1:1, 600 mL), washed with 1N HCl, water and brine, dried (MgSO4), and evaporated in vacuo. The residue was dissolved in MeOH-THF (3:1, 400 mL). To the solution was added an aqueous solution (100 mL) of K2CO3 (9.77 g) at 5° C., and the mixture was stirred at the same temperature for 1 hour. The organic solvent was evaporated, and the residue was adjusted to pH 2 by the addition of 3N HCl, and extracted with EtOAc. The organic layer was washed with water and brine, dried (MgSO4), and evaporated in vacuo. The residue was purified by silica gal column chromatography to give cis-4-(tert-butyldimethylsilyloxy)-N-benzyloxycarbonyl-D-proline (23.99 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660759B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-ce1db149d5d3404ab6fb24f15fa37f3a
출처 메모uspto-grants-2003_12