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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 886504생성일: 2026년 10월 27일

Hydrochloric Acid → (R)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propionic acid methyl ester

https://huagongshe.com/reaction/886504

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물1,4-DioxaneHCID 31275—
반응물Methyl (4R)-2,2-dimethyl-1,3-dioxolane-4-carboxylateHCID 853166—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물(R)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propionic acid methyl esterHCID 4503705463%

반응 단계

To a solution of (R)-2,2-dimethyl-[1,3]dioxolane-4-carboxylic acid methyl ester (2.5 g, 15.6 mmol) in methanol (15 mL) was added HCl in dioxane (4N, 5 mL, 20 mmol) and the reaction mixture was stirred at RT for 5 h. The reaction mixture was concentrated in vacuo, the resultant residue dissolved in THF (20 mL) and imidazole (1.28 g, 18.7 mmol) and tert-butylchlorodimethylsilane (2.47 g, 16.4 mmol) added. The reaction mixture was stirred at RT for 16 h. The reaction mixture was diluted with ethyl acetate (10 mL) and the mixture washed with water extracting with ethyl acetate (3×10 mL). The combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was subjected to flash chromatography (SiO2 gradient 0-50% EtOAc in cyclohexane) to yield (R)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propionic acid methyl ester as a colorless oil (2.29 g, 63%). 1H NMR (400 MHz, CDCl3) 4.26-4.20 (1H, m), 3.93 (1H, dd, J=10.1, 3.4 Hz), 3.86 (1H, dd, J=10.1, 2.8 Hz), 3.79 (3H, s), 3.01 (1H, d, J=7.8 Hz), 0.88 (9H, s), 0.06 (3H, s), 0.04 (3H, s)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08242104B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-89b0c610671346c1861b4953fad92c03
출처 메모uspto-grants-2012_08