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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1098151생성일: 2026년 10월 24일

Imidazole → (S)-methyl 2-(tert-butyldimethylsilyloxy)-3-((S)-1-methoxypropan-2-yloxy)propanoate

https://huagongshe.com/ko/reaction/1098151

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Magnesium perchlorateHCID 24840—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물(2S)-1-methoxypropan-2-olHCID 6993459—
반응물Methyl (2S)-2-oxiranecarboxylateHCID 10942355—
용매DimethylformamideHCID 6228—
생성물(S)-methyl 2-(tert-butyldimethylsilyloxy)-3-((S)-1-methoxypropan-2-yloxy)propanoateHCID 5927955730%

반응 조건

온도50 °C

반응 단계

Magnesium perchlorate (2.79 g, 12.49 mmol) was added in one portion to (S)-methyl oxirane-2-carboxylate (CAS no. 118712-39-3) (5.1 g, 49.96 mmol) and (S)-1-methoxypropan-2-ol (CAS no. 26550-55-0) (4.50 g, 49.96 mmol) at ambient temperature. The resulting suspension was stirred at 50° C. for 16 hours. The reaction mixture was diluted with DMF (50 mL) before adding 1H-imidazole (6.80 g, 99.92 mmol) and tert-butylchlorodimethylsilane (9.04 g, 59.95 mmol). The resulting solution was stirred at 40° C. for 5 hours. The reaction mixture was evaporated to dryness and re-dissolved in ethyl acetate (125 mL), and washed sequentially with water (50 mL) and saturated brine (25 mL). The organic layer was dried (MgSO4) and evaporated. The crude product was purified by flash silica chromatography, eluting with 0 to 50% ethyl acetate in isohexane to afford the product (4.52 g, 30%). 1H NMR (400 MHz, DMSO) δ 0.00 (d, 6H), 0.82 (s, 9H), 0.98 (d, 3H), 3.13-3.28 (m, 5H), 3.50-3.64 (m, 6H), 4.26-4.32 (m, 1H); m/z (ESI+) (M+H)+=307.19; HPLC tR=10.82 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143263B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-04c2d16591934da0ac7f45b270d3ce7b
출처 메모uspto-grants-2012_03