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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53459생성일: 2026년 10월 25일

Triethylamine → (E)-tert-Butyl 2-(2-methoxyethoxymethyl)-3-(p-toluenesulphonyl)acrylate

https://huagongshe.com/reaction/53459

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물p-Toluenesulphonyl iodideHCID 11022347—
반응물tert-Butyl 2-(2-methoxyethoxymethyl)acrylateHCID 11096016—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(E)-tert-Butyl 2-(2-methoxyethoxymethyl)-3-(p-toluenesulphonyl)acrylateHCID 10937543—

반응 단계

To a solution of p-toluenesulphonyl iodide (19.39 g, 68.7 mmol) in dichloromethane (50 mL) at room temperature under a nitrogen atmosphere was added tert-butyl 2-(2-methoxyethoxymethyl)acrylate (9.91 g, 45.8 mmol). The mixture was stirred at room temperature for 16 hours, cooled to 0° C. and triethylamine (12.7 mL, 91.6 mmol) added dropwise. The reaction was stirred at 0° C. for 0.5 hours and at room temperature for 4 hours, diluted with distilled water (100 mL) and the layers separated. The aqueous layer was further extracted with dichloromethane (25 mL) and the combined organic extracts were washed with 1.0M aqueous hydrochloric acid solution (100 mL), 5% aqueous sodium thiosulphate solution (25 mL) and distilled water (50 mL). The dichloromethane phase was concentrated under reduced pressure to give a brown oil (17.48 g, quantitative). The crude product was purified by chromatography on silica by gradient elution with hexane/ethyl acetate mixtues to give, after combination and evaporation of appropriate fractions, the title compound as a pale yellow oil (16.2 g, 95%) which crystallised on standing, m.pt.=40°-41° C., Rf =0.3 (silica; hexane/ethyl acetate, 2:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618970
출처 데이터셋uspto-grants-1997_04
ORD IDord-a856d0686a724180870dec869d279383
출처 메모uspto-grants-1997_04