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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1436158생성일: 2026년 10월 27일

Ethyl Acetate → tert-butyl {(S)-1-benzyloxymethyl-2-[2-oxo-2-(3,4,5-trifluorophenyl)ethoxy]ethyl}carbamate

https://huagongshe.com/reaction/1436158

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Ammonium ChlorideHCID 25517—
반응물1-Bromo-3,4,5-trifluorobenzeneHCID 611409—
반응물MagnesiumHCID 5462224—
반응물tert-butyl(S)-3-benzyloxymethyl-5-oxomorpholine-4-carboxylateHCID 67373012—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl {(S)-1-benzyloxymethyl-2-[2-oxo-2-(3,4,5-trifluorophenyl)ethoxy]ethyl}carbamateHCID 67373700—

반응 조건

온도40 °C

반응 단계

To a suspension of magnesium (249 mg) in diethyl ether (5 mL), 1-bromo-3,4,5-trifluorobenzene (446 μL) was added dropwise at 40° C. over 10 minutes, and the reaction solution was stirred at 40° C. for one hour. This solution was added dropwise to a solution of tert-butyl (S)-3-benzyloxymethyl-5-oxomorpholine-4-carboxylate (1.1 g) in tetrahydrofuran (30 mL) at −40° C. over 10 minutes, and the reaction solution was stirred at −40° C. for one hour. A saturated ammonium chloride solution was added to the solution in small portions at −40° C., and the reaction solution was returned to room temperature. Ethyl acetate was added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with brine, and then dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate system) to obtain 952 mg of the title compound. The property values of the compound are as follows.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618960B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-eab35ee9d8c0456c978732c08c61c567
출처 메모uspto-grants-2009_11